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Breton Village Pediatrics & Family Medicine

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Breton Village Pediatrics & Family Medicine is a clinic that specializes in Concierge Pediatrics and Concierge Family Medicine. The clinic is located in Grand Rapids, Michigan. Breton Village Pediatrics & Family Medicine is known for housing expert physicians. Breton Village Pediatrics & Family Medicine offers all the services, treatments and procedures pertinent to the specialties mentioned above.

2 Doctors | Website
About Breton Village Pediatrics & Family Medicine

"Breton Village Pediatrics & Family Medicine is a medical clinic for patients of all ages in Grand Rapids, Michigan. The practice takes a holistic, naturopathic approach to family medicine that extends beyond the limits of conventional health care. Peter Macfield, MD, and the team at Breton Village Pediatrics & Family Medicine emphasize the health of each patient as a whole person — not as a set of symptoms. 

Striving for optimal wellness for every patient, the team at Breton Village Pediatrics & Family Medicine is committed to medical care that helps free patients from a reliance on medications as much as possible. Their aim is to help patients live longer, with fewer diseases and health complaints. By offering integrative health care services designed to lower patients’ risks for medical complications, the practice promotes the optimal health, wellness, and longevity of each patient.

As a board-certified family practice provider, Dr. Macfield offers preventive care services and appropriate medical treatment for a broad range of health conditions at Breton Village Pediatrics & Family Medicine. He treats acute and chronic diseases, and provides geriatric care, immunizations, women’s health care, prenatal care, and weight management services.

Breton Village Pediatrics & Family Medicine accepts a variety of insurance plans. The practice also offers concierge medicine, a type of primary care that offers you more time with your doctor for a set fee. Call today or book a consultation online to find out more. "

Address

2460 Burton Street Southeast Suite 300, Grand Rapids,
MI 49546

Modes of Payment

Card | Cash


Providers
Filters
Peter Macfield - 2460 Burton Street Southeast, Grand Rapids, Michigan, 49546
Breton Village Pediatrics & Family Medicine
Concierge Family Medicine
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
2460 Burton Street Southeast, Suite 300, Grand Rapids, MI 49546
Masuma Macfield - 2460 Burton Street Southeast, Grand Rapids, Michigan, 49546
Breton Village Pediatrics & Family Medicine
Concierge Pediatrics
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
2460 Burton Street Southeast, Suite 300, Grand Rapids, MI 49546

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Conditions Treated
  • Muscle strains
  • High blood pressure
  • Rotator cuff
  • Anal fissure
  • Covid-19 testing
  • Allergies
  • Hemorrhoids
  • Concussion
  • Hyperthyroidism
  • Cervical cancer
  • Menopause
  • Chronic fatigue syndrome
  • Congestive heart failure
  • Acid reflux
  • Arrhythmias
  • Hypertension
  • Dementia
  • Hypothyroidism
  • Diabetes
  • Depression
  • Gout
  • Insomnia
  • Eating disorders
  • High cholesterol
  • Torticollis
  • Lactose intolerance
  • Kidney infection
  • Stroke
  • Kawasaki disease
  • Irritable bowel syndrome
  • Melanoma
  • Inguinal hernia
  • Swimmer's ear
  • Meningitis
  • Hydrocele
  • Hiatal hernia
  • Milia
  • Testicular torsion
  • Molluscum contagiosum
  • Hemangioma
  • Scleroderma
  • Multiple sclerosis
  • Harlequin ichthyosis
  • Scurvy
  • Narcolepsy
  • Nausea
  • Generalized anxiety disorder
  • Gallstones
  • Fifth disease
  • Tinea versicolor
  • Eczema
  • Osteomyelitis
  • Sepsis
  • Smallpox
  • Tourette syndrome
  • Diphtheria
  • Dermatitis
  • Deep vein thrombosis
  • Seizures
  • Cystic fibrosis
  • Ulcerative colitis
  • Cellulitis
  • Celiac disease
  • Umbilical hernia
  • Pityriasis rosea
  • Strep throat
  • Hand-foot-and-mouth disease
  • Ear infection
  • Croup
  • Cerebral palsy
  • Cardiomyopathy
  • Canker sore
  • Psoriasis
  • Back pain
  • Skin cancer
  • Pulmonary embolism
  • Atopic dermatitis
  • Asperger's syndrome
  • Rectal prolapse
  • Restless legs syndrome
  • Vitiligo
  • Rosacea
  • Roseola
  • Sarcoidosis
  • Sjogren's syndrome
  • Scarlet fever
  • Liver disease
  • Strabismus
  • Lupus
  • Autism spectrum disorder
  • Asthma
  • Adhd
  • Upper respiratory infection
  • Measles
  • Pneumonia
  • Acute pharyngitis
  • Allergic conjunctivitis
  • Allergic cough
  • Allergic rhinitis
  • Anhidrosis
  • Aniridia
  • Attention deficit disorder (add)
  • Attention deficit hyperactivity disorder
  • Bacterial pneumonia
  • Bad breath
  • Beriberi
  • Black hairy tongue
  • Burning mouth syndrome
  • Candidiasis
  • Carbuncle
  • Castleman disease
  • Cat scratch disease
  • Central sleep apnea
  • Cherry angioma
  • Chikungunya
  • Cholera
  • Cholesteatoma
  • Chronic bronchitis
  • Chronic cough
  • Chronic headache
  • Chronic illness
  • Chronic obstructive pulmonary disease
  • Chronic pain
  • Chronic sinusitis
  • Cold urticaria
  • Comedones
  • Coronary artery disease
  • Coronary heart disease
  • Crooked teeth
  • Cyclic vomiting syndrome
  • De quervain's
  • Delayed ejaculation
  • Dengue fever
  • Dermatitis herpetiformis
  • Dermatomyositis
  • Desmoid tumor
  • Deviated nasal septum
  • Dextrocardia
  • Diabetes insipidus
  • Diabetes mellitus
  • Diabetic foot ulcers
  • Diabetic neuropathy
  • Diabetic retinopathy
  • Diaphragmatic hernia
  • Digeorge syndrome
  • Dilated cardiomyopathy
  • Diphallia
  • Diplopia
  • Disseminated intravascular coagulation
  • Distal radius fracture
  • Donovanosis
  • Dravet syndrome
  • Droopy eyelids
  • Drowsiness
  • Dry eye
  • Dry mouth
  • Dysarthria
  • Dysgraphia
  • Dysplasia
  • Dysplastic nevus
  • Ebstein's anomaly
  • Eclampsia
  • Ectodermal dysplasias
  • Ectropion
  • Ehrlichiosis
  • Elbow dislocation
  • Elbow pain
  • Empyema
  • Encephalocele
  • Encopresis
  • Endocarditis
  • Endometrial cancer
  • Endometrial polyps
  • Endometritis
  • Endophthalmitis
  • Enlarged liver
  • Enlarged prostate
  • Entropion
  • Eosinophilic esophagitis
  • Epicanthal folds
  • Epidermoid cyst
  • Epidermolysis bullosa
  • Epidural hematoma
  • Episcleritis
  • Epispadias
  • Erysipelas
  • Erythema multiforme
  • Erythema nodosum
  • Erythromelalgia
  • Eschar
  • Esophageal atresia
  • Esophageal varices
  • Esotropia
  • Essential thrombocythemia
  • Essential tremor
  • Ewing sarcoma
  • Exercise induced asthma
  • Exocrine pancreatic insufficiency
  • Eye allergies
  • Eyelid bump
  • Eyestrain
  • Fabry disease
  • Fainting
  • Familial hypercholesterolemia
  • Farsightedness
  • Fatal familial insomnia
  • Fecal impaction
  • Fecal incontinence
  • Femoral hernia
  • Fibroadenoma
  • Fibrocystic breast disease
  • Fibromuscular dysplasia
  • Fibrous dysplasia
  • Flat feet
  • Folate deficiency
  • Follicular lymphoma
  • Food allergy
  • Food intolerance
  • Foot drop
  • Foot pain
  • Friedreich ataxia
  • Frontotemporal dementia
  • Frozen shoulder
  • Fungal infections
  • Galactosemia
  • Gallbladder cancer
  • Gallbladder disease
  • Gardner syndrome
  • Gastrectomy
  • Gastroesophageal reflux disease (gerd)
  • Gastrointestinal bleeding
  • Gaucher disease
  • Giant cell arteritis
  • Gigantism
  • Gilbert syndrome
  • Gingivostomatitis
  • Glomerulonephritis
  • Glossitis
  • Goodpasture syndrome
  • Granuloma annulare
  • Granulomatosis with polyangiitis
  • Grief
  • Groin pain
  • Grover's disease
  • Growth hormone deficiency
  • Gum disease
  • Guttate psoriasis
  • Hair loss
  • Hairy cell leukemia
  • Hashimoto thyroiditis
  • Head lice
  • Hearing loss
  • Heart block
  • Heart disease
  • Heart failure
  • Heart health
  • Heart transplant
  • Heel spurs
  • Hellp syndrome
  • Hemiplegia
  • Hemochromatosis
  • Hemolysis
  • Hemolytic anemia
  • Hemolytic uremic syndrome
  • Hemophilia a
  • Hemorrhagic stroke
  • Henoch schonlein purpura
  • Hepatorenal syndrome
  • Hereditary angioedema
  • Herpangina
  • Herpes zoster
  • High potassium level
  • High risk pregnancy
  • Hip arthritis
  • Hip fractures
  • Hirschsprung disease
  • Hiv aids
  • Holoprosencephaly
  • Horner syndrome
  • Horseshoe kidney
  • Human papillomavirus infection
  • Hydatidiform mole
  • Hydranencephaly
  • Hydronephrosis
  • Hydrops fetalis
  • Hyperaldosteronism
  • Hypercalcemia
  • Hyperemesis gravidarum
  • Hyperhidrosis
  • Hyperopia
  • Hyperparathyroidism
  • Hypertrophic cardiomyopathy
  • Hyperventilation
  • Hyphema
  • Hypogonadism
  • Hypoparathyroidism
  • Hypophosphatasia
  • Hypophosphatemia
  • Hypopituitarism
  • Hypoplastic left heart syndrome
  • Hypospadias
  • Hypothermia
  • Hypotonia
  • Hypovolemic shock
  • Ichthyosis vulgaris
  • Idiopathic pulmonary fibrosis
  • Idiopathic thrombocytopenic purpura
  • Iga nephropathy
  • Ileostomy
  • Inclusion body myositis
  • Infertility
  • Inflammatory bowel disease
  • Inflammatory breast cancer
  • Influenza
  • Interstitial cystitis
  • Interstitial lung disease
  • Intertrigo
  • Intrauterine growth restriction
  • Intussusception
  • Iron deficiency anemia
  • Ischemic heart disease
  • Ischemic stroke
  • Joint pain
  • Juvenile dermatomyositis
  • Juvenile idiopathic arthritis
  • Kabuki syndrome
  • Kallmann syndrome
  • Kaposi sarcoma
  • Keratitis
  • Keratoconus
  • Kidney cancer
  • Kidney disease
  • Kidney transplant
  • Klippel feil syndrome
  • Knee arthritis
  • Knee injury
  • Knock knees
  • Krabbe disease
  • Kwashiorkor
  • Labral tears
  • Labyrinthitis
  • Langerhans cell histiocytosis
  • Laryngeal cancer
  • Laryngectomy
  • Laryngomalacia
  • Lateral epicondylitis
  • Lazy eye
  • Leg pain
  • Legg calve perthes disease
  • Legionnaire disease
  • Leiomyosarcoma
  • Leishmaniasis
  • Lemierre syndrome
  • Lennox gastaut syndrome
  • Leptospirosis
  • Lesch nyhan syndrome
  • Leukocytosis
  • Leukoplakia
  • Li fraumeni syndrome
  • Lichen sclerosis
  • Lichen simplex chronicus
  • Lipedema
  • Liposarcoma
  • Lissencephaly
  • Livedo reticularis
  • Liver cancer
  • Liver failure
  • Liver spots
  • Liver transplant
  • Long qt syndrome
  • Loose teeth
  • Lordosis
  • Low blood sugar
  • Low sodium level
  • Low testosterone
  • Ludwig angina
  • Lumbar radiculopathy
  • Lumbar spondylosis
  • Lung adenocarcinoma
  • Lung cancer
  • Lung nodules
  • Lungs
  • Lupus nephritis
  • Lymphadenitis
  • Lymphangitis
  • Lymphocytic colitis
  • Lymphogranuloma venereum
  • Lynch syndrome
  • Macrosomia
  • Magnesium deficiency
  • Major depressive disorder
  • Malabsorption
  • Male breast cancer
  • Male pattern baldness
  • Malignant hyperthermia
  • Malnutrition
  • Mantle cell lymphoma
  • Maple syrup urine disease
  • Mastectomy
  • Mastoiditis
  • May thurner syndrome
  • Mcl injury
  • Meckel diverticulum
  • Medial epicondylitis
  • Medulloblastoma
  • Melioidosis
  • Memory loss
  • Men's health
  • Menorrhagia
  • Mental illness
  • Merkel cell carcinoma
  • Metabolic acidosis
  • Metabolic syndrome
  • Metatarsalgia
  • Meth addiction
  • Methemoglobinemia
  • Mitral regurgitation
  • Mitral valve prolapse
  • Mitral valve regurgitation
  • Mittelschmerz
  • Mixed connective tissue disease
  • Mood disorders
  • Morgellons disease
  • Morning sickness
  • Morphea
  • Mouth sores
  • Mucormycosis
  • Mumps
  • Munchausen syndrome by proxy
  • Mycoplasma pneumonia
  • Necrosis
  • Nephrotic syndrome
  • Neuralgia
  • New daily persistent headache
  • Non alcoholic fatty liver disease
  • Nummular eczema
  • Obsessive compulsive disorder
  • Obstructive sleep apnea
  • Ogilvie syndrome
  • Oral herpes
  • Orchitis
  • Orthostatic hypotension
  • Osteomalacia
  • Otitis
  • Otitis media
  • Overactive bladder
  • Painful swallowing
  • Panic disorder
  • Parainfluenza
  • Paroxysmal supraventricular tachycardia
  • Pellagra
  • Pelvic pain
  • Pemphigus
  • Pemphigus vulgaris
  • Peptic ulcer
  • Peptic ulcer disease
  • Peripheral vascular disease
  • Pertussis
  • Pinched nerves
  • Pityriasis alba
  • Plaque psoriasis
  • Polymorphous light eruption
  • Polymyalgia rheumatica
  • Portal hypertension
  • Post traumatic stress disorder
  • Premenstrual syndrome
  • Primary care
  • Proctitis
  • Protein deficiency
  • Pubic lice
  • Pulmonary edema
  • Pulmonary fibrosis
  • Purpura
  • Quitting smoking
  • Rectal
  • Reye syndrome
  • Rubella
  • Sacroiliac joint pain
  • Septicemia
  • Serum sickness
  • Sexual health
  • Sexually transmitted diseases
  • Shortness of breath
  • Situs inversus
  • Sleep disorders
  • Splenomegaly
  • Sprains
  • Stress management
  • Subcutaneous emphysema
  • Suicidal ideation
  • Superficial thrombophlebitis
  • Thrombophlebitis
  • Trimethylaminuria
  • Vasoconstriction
  • Vitamin b12 deficiency
  • Women's health
  • Yellow fever
  • Acrogeria
  • Acute conjunctivitis
  • Acute cystitis
  • Acute glaucoma
  • Acute mountain sickness
  • Acute sinusitis
  • Add adhd
  • Aging well
  • Alcohol dependence
  • Anencephaly
  • Apert syndrome
  • Aphantasia
  • Apraxia
  • Beckwith wiedemann syndrome
  • Birthmarks
  • Blount disease
  • Brachydactyly
  • Cafe au lait spots
  • Caput succedaneum
  • Caudal regression syndrome
  • Cerebellar hypoplasia
  • Choanal atresia
  • Clubfoot
  • Congenital adrenal hyperplasia
  • Congenital diaphragmatic hernia
  • Congenital heart disease
  • Cornelia de lange syndrome
  • Craniosynostosis
  • Cri du chat syndrome
  • Crouzon syndrome
  • Cystic hygroma
  • Cystinosis
  • Dandy walker syndrome
  • Duchenne muscular dystrophy
  • Erb's palsy
  • Fanconi anemia
  • Fragile x syndrome
  • Gastroschisis
  • Hermansky pudlak syndrome
  • Microcephaly
  • Micrognathia
  • Microtia
  • Moebius syndrome
  • Myelomeningocele
  • Necrotizing enterocolitis
  • Neonatal abstinence syndrome
  • Neuroblastoma
  • Newborn jaundice
  • Noma
  • Noonan syndrome
  • Omphalocele
  • Osgood schlatter disease
  • Osteogenesis imperfecta
  • Patent ductus arteriosus
  • Pectus carinatum
  • Pectus excavatum
  • Pfeiffer syndrome
  • Phenylketonuria
  • Plagiocephaly
  • Poland syndrome
  • Polydactyly
  • Pompe disease
  • Precocious puberty
  • Progeria
  • Rett syndrome
  • Rhabdomyosarcoma
  • Rheumatic fever
  • Rickets
  • Selective mutism
  • Sotos syndrome
  • Spinal muscular atrophy
  • Stickler syndrome
  • Stork bite
  • Sturge weber syndrome
  • Sudden infant death syndrome
  • Syndactyly
  • Tay sachs disease
  • Temper tantrums
  • Tetralogy of fallot
  • Thalassemia
  • Treacher collins syndrome
  • Truncus arteriosus
  • Tuberous sclerosis
  • Uncombable hair syndrome
  • Undescended testicle
  • Ventricular septal defects
  • Wilms tumor
  • Aarskog syndrome
  • Abo incompatibility
  • Acrodermatitis enteropathica
  • Acute flaccid myelitis
  • Acute otitis externa
  • Adams oliver syndrome
  • Adenosine deaminase deficiency
  • Adrenoleukodystrophy
  • Aicardi goutieres syndrome
  • Aicardi syndrome
  • Albright's hereditary osteodystrophy
  • Alexander disease
  • Cramps
  • Sore throat
  • Alopecia totalis
  • Alopecia universalis
  • Alternating hemiplegia of childhood
  • Amebiasis
  • Anaplastic large cell lymphoma
  • Angiodysplasia of the colon
  • Angioimmunoblastic t cell lymphoma
  • Aphthous stomatitis
  • Arachnodactyly
  • Athetosis
  • Carotid stenosis
  • Carpenter syndrome
  • Cartilage hair hypoplasia
  • Cat eye syndrome
  • Cavernous sinus thrombosis
  • Central pain syndrome
  • Central serous chorioretinopathy
  • Cerebellar degeneration
  • Cerebral amyloid angiopathy
  • Cerebral cavernous malformation
  • Cerebral hypoxia
  • Cervical disc herniations
  • Cervical spinal stenosis
  • Cervical spine disorders
  • Char syndrome
  • Chediak higashi syndrome
  • Cheilitis glandularis
  • Chemical pneumonitis
  • Cherubism
  • Chiari malformation type 2
  • Cloudy cornea
  • Cmv retinitis
  • Coats disease
  • Cockayne syndrome
  • Coffin lowry syndrome
  • Coffin siris syndrome
  • Cogan's syndrome
  • Cohen syndrome
  • Cold and flu
  • Cold flu
  • Collagenous colitis
  • Coloboma of iris
  • Colorado tick fever
  • Cone rod dystrophy
  • Congenital cataract
  • Congenital generalized lipodystrophy
  • Congenital hyperinsulinism
  • Congenital hypothyroidism
  • Congenital lobar emphysema
  • Congenital myasthenic syndrome
  • Congenital syphilis
  • Congenital toxoplasmosis
  • Constrictive pericarditis
  • Cor triatriatum
  • Corns and calluses
  • Coronary artery spasm
  • Corpus callosum agenesis
  • Cortical dysplasia
  • Corticobasal degeneration
  • Costello syndrome
  • Cowden syndrome
  • Cramp fasciculation syndrome
  • Craniodiaphyseal dysplasia
  • Craniopharyngioma
  • Craniotabes
  • Crigler najjar syndrome
  • Crowded teeth
  • Cryptococcal meningitis
  • Medication management
  • Meds
  • Family conflict
  • Foot health
  • Idiopathic edema
  • Prescription drug addiction
  • Ring chromosome 18
  • Short philtrum
  • Clubbing of the fingers or toes
  • Happy and healthy holidays
  • Symptoms and conditions
  • Apnea of prematurity
  • Atrioventricular septal defect
  • Benign rolandic epilepsy
  • Bronchopulmonary dysplasia
  • Bulging fontanelles
  • Childhood disintegrative disorder
  • Chondrodysplasia
  • Cleft lip and palate
  • Cleft palate and cleft lip
  • Cloacal exstrophy
  • Cutis marmorata telangiectatica congenita
  • Cyclic neutropenia
  • Cytomegalovirus infection
  • Donnai barrow syndrome
  • Duodenal atresia
  • Dystrophic epidermolysis bullosa
  • Ear tag
  • Eec syndrome
  • Eisenmenger syndrome
  • Ellis van creveld syndrome
  • Emery dreifuss muscular dystrophy
  • Endocardial cushion defect
  • Enlarged adenoids
  • Epidermolysis bullosa simplex
  • Evans syndrome
  • Exstrophy of the bladder
  • Fanconi syndrome
  • Fetal hydantoin syndrome
  • Floating harbor syndrome
  • Foxg1 syndrome
  • Fraser syndrome
  • Freeman sheldon syndrome
  • Frontonasal dysplasia
  • Fumarase deficiency
  • Ganglioneuroma
  • Gianotti crosti syndrome
  • Giant congenital melanocytic nevus
  • Glucose 6 phosphate dehydrogenase deficiency
  • Glutaric acidemia type 1
  • Gm1 gangliosidosis
  • Grass allergy
  • Hallermann streiff syndrome
  • Hemihyperplasia
  • Hemimegalencephaly
  • Hemolytic disease of the newborn
  • Hemophagocytic lymphohistiocytosis
  • Hemophilia b
  • Hepatoblastoma
  • Hereditary spherocytosis
  • Heterotaxy syndrome
  • Holt oram syndrome
  • Hypochondroplasia
  • Hypohidrotic ectodermal dysplasia
  • Hypomelanosis of ito
  • Imperforate anus
  • Incontinentia pigmenti
  • Infant botulism
  • Infantile pyloric stenosis
  • Infectious mononucleosis
  • Interrupted aortic arch
  • Jacobsen syndrome
  • Juvenile myoclonic epilepsy
  • Kohler disease
  • Koolen de vries syndrome
  • Landau kleffner syndrome
  • Laryngeal cleft
  • Linear nevus sebaceous syndrome
  • Lowe syndrome
  • Meatal stenosis
  • Meconium aspiration syndrome
  • Meningocele
  • Meningococcemia
  • Menkes disease
  • Menkes syndrome
  • Metopic ridge
  • Miller dieker syndrome
  • Miller syndrome
  • Mongolian blue spots
  • Muenke syndrome
  • Myoclonic epilepsy
  • Myotonia congenita
  • Nail patella syndrome
  • Nasal flaring
  • Nemaline myopathy
  • Neonatal conjunctivitis
  • Neonatal herpes
  • Neonatal sepsis
  • Nephrogenic diabetes insipidus
  • Nephronophthisis
  • Netherton syndrome
  • Neuronal ceroid lipofuscinoses
  • Newborn low blood sugar
  • Newborn transient tachypnea
  • Niemann pick disease
  • Otitis media with effusion
  • Periventricular leukomalacia
  • Pfapa
  • Pierre robin sequence
  • Pitt hopkins syndrome
  • Pituitary dwarfism
  • Polymicrogyria
  • Pontocerebellar hypoplasia
  • Porencephaly
  • Potocki lupski syndrome
  • Potter syndrome
  • Propionic acidemia
  • Prune belly syndrome
  • Pulmonary atresia
  • Pulmonary valve stenosis
  • Rasmussen encephalitis
  • Retinopathy of prematurity
  • Rhabdoid tumor
  • Rhabdomyosarcoma embryonal
  • Roberts syndrome
  • Robinow syndrome
  • Rubinstein taybi syndrome
  • Saethre chotzen syndrome
  • Scalded skin syndrome
  • Seckel syndrome
  • Severe combined immunodeficiency
  • Short stature
  • Single palmar crease
  • Sirenomelia
  • Slipped capital femoral epiphysis
  • Small for gestational age
  • Smith lemli opitz syndrome
  • Smith magenis syndrome
  • Spinal muscular atrophy type 1
  • Spondyloepiphyseal dysplasia
  • Sprengel deformity
  • Stereotypic movement disorder
  • Sunken fontanelles
  • Supravalvular aortic stenosis
  • Tetrasomy x
  • Thanatophoric dysplasia
  • Torch syndrome
  • Total anomalous pulmonary venous return
  • Toxic synovitis
  • Toxocariasis
  • Tracheobronchomalacia
  • Tracheoesophageal fistula
  • Transient tic disorder
  • Transposition of the great arteries
  • Tricuspid atresia
  • Triple x syndrome
  • Trisomy 14 mosaicism
  • Twin to twin transfusion syndrome
  • Vacterl association
  • Velopharyngeal insufficiency
  • Von gierke disease
  • Wagr syndrome
  • Weaver syndrome
  • West syndrome
  • Wiedemann steiner syndrome
  • Zellweger syndrome
  • Acalvaria
  • Achondrogenesis
  • Acrodysostosis
  • Acute bronchiolitis
  • Acute cerebellar ataxia
  • Adenylosuccinate lyase deficiency
  • Aec syndrome
  • Allan herndon dudley syndrome
  • Alpers huttenlocher syndrome
  • Alpha mannosidosis
  • Andersen disease
  • Aortopulmonary window
  • Arginase deficiency
  • Argininosuccinic aciduria
  • Arterial tortuosity syndrome
  • Aspartylglucosaminuria
  • Asphyxiating thoracic dystrophy
  • Aural polyps
  • Baller gerold syndrome
  • Bannayan riley ruvalcaba syndrome
  • Bartsocas papas syndrome
  • Behr syndrome
  • Beta ketothiolase deficiency
  • Bilirubin encephalopathy
  • Childhood pancreatitis
  • Chromosome 22 duplication
  • Chromosome 8p deletion
  • Classic galactosemia
  • Colonic atresia
  • Congenital anomalies of the heart
  • Congenital central hypoventilation syndrome
  • Congenital cytomegalovirus
  • Congenital heart block
  • Congenital hepatic fibrosis
  • Congenital mesoblastic nephroma
  • Congenital mirror movement disorder
  • Congenital nephrotic syndrome
  • Congenital radioulnar synostosis
  • Congenital sucrase isomaltase deficiency
  • Congenital tracheomalacia
  • Cytomegalic inclusion disease
  • Delayed growth
  • Diencephalic syndrome
  • Door syndrome
  • Dopa responsive dystonia
  • Double outlet left ventricle
  • Dubowitz syndrome
  • Duplication of urethra
  • Early infantile epileptic encephalopathy
  • Embryonal tumor with multilayered rosettes
  • Endocardial fibroelastosis
  • Fanconi bickel syndrome
  • Feingold syndrome
  • Femoral facial syndrome
  • Fetal cystic hygroma
  • Fg syndrome
  • Fryns syndrome
  • Fucosidosis
  • Gaba transaminase deficiency
  • Galactokinase deficiency
  • Galactosialidosis
  • Galloway mowat syndrome
  • Ganglioneuroblastoma
  • Gangliosidosis
  • Gastroesophageal reflux in infants
  • Gaucher disease type 2
  • Gaucher disease type 3
  • Geleophysic dysplasia
  • Giant congenital nevus
  • Glutaric acidemia type 2
  • H influenzae meningitis
  • Hennekam syndrome
  • Holocarboxylase synthetase deficiency
  • Icf syndrome
  • Idiopathic neutropenia
  • Idiopathic pulmonary hemosiderosis
  • Infant hearing loss
  • Infantile apnea
  • Infantile digital fibromatosis
  • Infantile myofibromatosis
  • Intestinal pseudo obstruction
  • Intraventricular hemorrhage of the newborn
  • Isovaleric acidemia
  • Jackson weiss syndrome
  • Johanson blizzard syndrome
  • Junctional epidermolysis bullosa
  • Juvenile myelomonocytic leukemia
  • Juvenile temporal arteritis
  • Kaufman oculocerebrofacial syndrome
  • Kerion celsi
  • Kindler syndrome
  • Kniest dysplasia
  • Knobloch syndrome
  • L1 syndrome
  • Lactate dehydrogenase deficiency
  • Lambdoid synostosis
  • Langer mesomelic dysplasia
  • Leri weill dyschondrosteosis
  • Lung agenesis
  • Mandibuloacral dysplasia
  • Marcus gunn phenomenon
  • Marden walker syndrome
  • Marinesco sjogren syndrome
  • Marshall smith syndrome
  • Marshall syndrome
  • Mass phenotype
  • Mckusick kaufman syndrome
  • Meckel syndrome
  • Medium chain acyl coa dehydrogenase deficiency
  • Megalencephaly capillary malformation syndrome
  • Meier gorlin syndrome
  • Mitral atresia
  • Mosaic trisomy 7
  • Mosaic trisomy 8
  • Mosaic trisomy 9
  • Mucolipidosis type 4
  • Mucopolysaccharidosis type 1
  • Mucopolysaccharidosis type 2
  • Mucopolysaccharidosis type 3
  • Myhre syndrome
  • Neonatal hemochromatosis
  • Neonatal hypothyroidism
  • Neonatal onset multisystem inflammatory disease
  • Newborn head molding
  • Newborn polycythemia
  • Nicolaides baraitser syndrome
  • Nijmegen breakage syndrome
  • Ohdo syndrome
  • Opitz g bbb syndrome
  • Opsoclonus myoclonus syndrome
  • Pallister hall syndrome
  • Pallister killian mosaic syndrome
  • Paroxysmal cold hemoglobinuria
  • Pediatric brain tumors
  • Pediatric myocarditis
  • Pediatric obesity
  • Peer relationships
  • Peho syndrome
  • Penoscrotal transposition
  • Pentasomy x
  • Perianal streptococcal cellulitis
  • Periventricular heterotopia
  • Perlman syndrome
  • Peters plus syndrome
  • Pik3ca related overgrowth spectrum
  • Pili torti
  • Pilonidal sinus disease
  • Pinealectomy
  • Pityriasis lichenoides et varioliformis acuta
  • Platelet storage pool deficiency
  • Pleuropulmonary blastoma
  • Popliteal pterygium syndrome
  • Post traumatic epilepsy
  • Prekallikrein deficiency
  • Premature infant
  • Primary amebic meningoencephalitis
  • Primary carnitine deficiency
  • Primitive neuroectodermal tumor
  • Progressive myoclonic epilepsy
  • Puberty disorder
  • Pulmonary atresia with intact ventricular septum
  • Pyridoxine deficiency
  • Pyruvate carboxylase deficiency
  • Rapadilino syndrome
  • Renpenning syndrome
  • Right ventricle hypoplasia
  • Rothmund thomson syndrome
  • Russell silver dwarfism
  • Satoyoshi syndrome
  • Scalp ear nipple syndrome
  • Schimke immuno osseous dysplasia
  • Schindler disease
  • Schinzel giedion syndrome
  • Schwartz jampel syndrome
  • Sea blue histiocytosis
  • Secondary immunodeficiency
  • Severe congenital neutropenia
  • Short chain acyl coa dehydrogenase deficiency
  • Short qt syndrome
  • Short syndrome
  • Sialidosis
  • Simpson golabi behmel syndrome
  • Sjogren larsson syndrome
  • Smith kingsmore syndrome
  • Snyder robinson syndrome
  • Spinal muscular atrophy type 2
  • Spinal muscular atrophy type 3
  • Spondylocostal dysostosis
  • Spondyloepiphyseal dysplasia congenita
  • Sternal cleft
  • Stuve wiedemann syndrome
  • Subvalvular aortic stenosis
  • Temple syndrome
  • Tetra amelia syndrome
  • Tetrasomy 9p
  • Thrombocytopenia absent radius syndrome
  • Townes brocks syndrome
  • Tracheal agenesis
  • Transient erythroblastopenia of childhood
  • Trisomy 2 mosaicism
  • Van maldergem syndrome
  • Vici syndrome
  • Visceral larva migrans
  • Visceromegaly
  • Wiedemann rautenstrauch syndrome
  • And breastfeeding
  • Anomalous left coronary artery from the pulmonary artery
  • Anophthalmia plus syndrome
  • Arrhinia
  • Arterial calcification of infancy
  • Asphyxia neonatorum
  • Atresia of small intestine
  • Ballinger wallace syndrome
  • Beare stevenson cutis gyrata syndrome
  • Benign familial neonatal seizures
  • Berdon syndrome
  • Beta mannosidosis
  • Bowen conradi syndrome
  • C syndrome
  • Carey fineman ziter syndrome
  • Charlie m syndrome
  • Childhood acute myeloid leukemia
  • Childhood hypophosphatasia
  • Childhood iron deficiency anemia
  • Childhood volvulus
  • Cln1 disease
  • Cln3 disease
  • Cln5 disease
  • Cockayne syndrome type 2
  • Cold induced sweating syndrome
  • Coloboma of eye lens
  • Congenital afibrinogenemia
  • Congenital aplastic anemia
  • Congenital contractures
  • Congenital femoral deficiency
  • Congenital fiber type disproportion
  • Congenital fibrinogen deficiency
  • Congenital generalized fibromatosis
  • Congenital hemolytic anemia
  • Congenital herpes simplex
  • Congenital lipoid adrenal hyperplasia
  • Congenital microcoria
  • Congenital mitral stenosis
  • Congenital mumps
  • Congenital muscular dystrophy type 1a
  • Congenital nonhemolytic jaundice
  • Congenital plasminogen deficiency
  • Congenital pulmonary lymphangiectasia
  • Cranioectodermal dysplasia
  • Craniofacial deafness hand syndrome
  • Cryptosporidium enteritis
  • Curry jones syndrome
  • Cystic adenomatoid malformation of lung
  • Cytochrome p450 oxidoreductase deficiency
  • Cytoplasmic body myopathy
  • Dehydrated hereditary stomatocytosis
  • Desbuquois syndrome
  • Developmental expressive language disorder
  • Developmental reading disorder
  • Diffuse mesangial sclerosis
  • Dihydropteridine reductase deficiency
  • Distal 18q deletion syndrome
  • Encephalocele anencephaly
  • Epilepsy with myoclonic atonic seizures
  • Exstrophy epispadias complex
  • Familial glucocorticoid deficiency
  • Familial hypopituitarism
  • Familial paroxysmal nonkinesigenic dyskinesia
  • Familial porencephaly
  • Farber lipogranulomatosis
  • Fetal akinesia sequence
  • Fetal and neonatal alloimmune thrombocytopenia
  • Fetal edema
  • Fetal thalidomide syndrome
  • Filippi syndrome
  • Fountain syndrome
  • Frank ter haar syndrome
  • Galactose epimerase deficiency
  • Gemss syndrome
  • Genetic epilepsy with febrile seizures plus
  • Genital dwarfism
  • Gorlin chaudhry moss syndrome
  • Hardikar syndrome
  • Hemangioma thrombocytopenia syndrome
  • Hemophilia a or b
  • Hereditary hypophosphatemic rickets
  • High blood pressure in infants
  • Histidinemia
  • Homocystinuria due to mthfr deficiency
  • Horizontal gaze palsy with progressive scoliosis
  • Hydrocephalus due to congenital stenosis of aqueduct of sylvius
  • Hygroma cervical
  • Hyperlysinemia
  • Hypochondrogenesis
  • Inborn amino acid metabolism disorder
  • Increased head circumference
  • Infant hyperglycemia
  • Infantile onset spinocerebellar ataxia
  • Isolated growth hormone deficiency
  • Microcephalic osteodysplastic primordial dwarfism type 1
  • Microcephalic osteodysplastic primordial dwarfism type 2
  • Mucolipidosis 3
  • Mucopolysaccharidosis type 3a
  • Mucopolysaccharidosis type 3b
  • Mucopolysaccharidosis type 4
  • Mucopolysaccharidosis type 4a
  • Mucopolysaccharidosis type 6
  • Mucopolysaccharidosis type 7
  • Mulibrey nanism
  • Neonatal ovarian cyst
  • Neonatal severe hyperparathyroidism
  • Nonbullous congenital ichthyosiform erythroderma
  • Oculocerebrocutaneous syndrome
  • Omphalomesenteric cyst
  • Oppenheim dystonia
  • Ornithine translocase deficiency
  • Orofaciodigital syndrome 1
  • Orotic aciduria type 1
  • Overhydrated hereditary stomatocytosis
  • Palatopharyngeal incompetence
  • Paris trousseau thrombocytopenia
  • Partial atrioventricular canal
  • Pena shokeir syndrome type 2
  • Peroxisomal acyl coa oxidase deficiency
  • Pgm1 cdg
  • Phacomatosis pigmentokeratotica
  • Phacomatosis pigmentovascularis
  • Phosphoglycerate kinase deficiency
  • Phosphoglycerate mutase deficiency
  • Pmm2 congenital disorder of glycosylation
  • Potassium aggravated myotonia
  • Primary intestinal lymphangiectasia
  • Pulmonary atresia with ventricular septal defect
  • Rubella or measles
  • Toriello carey syndrome
  • Transient neonatal diabetes mellitus
  • Trisomy 12 mosaicism
  • Trisomy 17 mosaicism
  • Trisomy 3 mosaicism
  • Walker dyson syndrome
  • X linked creatine deficiency
  • X linked infantile spinal muscular atrophy
  • X linked intellectual disability
  • X linked severe combined immunodeficiency
  • Yunis varon syndrome
  • Ulcers
  • Primary immunodeficiency
  • Monkeypox
more..
Treatments & Procedures
  • Blood pressure medication
  • Physical examination
  • Immunizations and vaccinations
  • Mole removal
  • Stitch removal
  • Well child visits
  • Pap smear
  • Sprains
  • Joint injections
  • Skin biopsies
  • Cancer screening
  • Annual wellness exam
  • Chronic care management
  • Care coordination
  • Blood tests
  • Pediatric urgent care
  • Vaccines
  • Circumcision
  • Ear tubes
  • Immunization
  • Mental health counseling
  • Lumbar puncture
  • Pediatric laproscopy
  • Pediatric thoracoscopy
  • Medical ear piercing
  • Tetralogy of fallot repair
  • Tof repair
  • Pediatric sleep problems
  • Prematurity and low birth weight
  • Oral examination
  • Point of care a1c
  • Well woman care
  • Behavioral health evaluation
  • Drug and alcohol addiction treatment
  • Semaglutide
more..
Additional Services
  • Weight Loss

Frequently Asked Questions

Where is Breton Village Pediatrics & Family Medicine located?

Breton Village Pediatrics & Family Medicine is located in 2460 Burton Street Southeast Suite 300, Grand Rapids, MI 49546.

What are the various modes of payment does Breton Village Pediatrics & Family Medicine Accept?

Breton Village Pediatrics & Family Medicine accepts Card | Cash.

What are the doctors who practice in Breton Village Pediatrics & Family Medicine specialize in?

Currently there are around 2 providers practice in Breton Village Pediatrics & Family Medicine who specialise in Concierge Pediatrics and Concierge Family Medicine, etc

How can I make appointments with doctors in Breton Village Pediatrics & Family Medicine?

You can take appointments for doctors who practice in Breton Village Pediatrics & Family Medicine online on their website or by calling them.

Location