clinic

Pinnacle Pediatrics

5 Stars (9 Reviews)

Pinnacle Pediatrics is a clinic that specializes in Concierge Pediatrics. The clinic is located in Sewickley, Pennsylvania. Pinnacle Pediatrics is known for housing expert physicians. Pinnacle Pediatrics offers all the services, treatments and procedures pertinent to the specialties mentioned above.

1 Doctor | Website
Overview
Providers
Reviews
Services
Location
About Pinnacle Pediatrics

"Pinnacle Pediatrics the pediatric practice of Dr. Scott Serbin, combines the highest quality pediatric health care with unmatched service and convenience. This is a “concierge” style practice – the first in Western Pennsylvania and the first pediatric “concierge” practice in the country.

Please browse our website to learn more about our practice and its many advantages. For those families who view their children's health and well-being as the most important aspect of their lives, Pinnacle Pediatrics provides the ultimate pediatric health care experience."

Address

1606 Twin Oaks Drive Sewickley, PA 15143 Sewickley,
PA 15143

Modes of Payment

Card | Cash

Providers
Scott Serbin - 1606 Twin Oaks Drive Sewickley, PA 15143, Sewickley, Pennsylvania, 15143
Scott Serbin, MD
Pinnacle Pediatrics
Concierge Pediatrics
(9)
Fee $25 - $100
Max no. of Patients: 500
Accepting New Patients: NA
1606 Twin Oaks Drive Sewickley, PA 15143, Sewickley, PA 15143
Message
Call
Website
Reviews
Posted by FMDD User
February 10, 2023
Kind and caring professional who truly listens to my eight-year-old babble away.

Review For Scott Serbin

Posted by FMDD User
January 13, 2023
Dr. Serbin is not only a superb doctor, but he also has excellent instincts and maintains his cool under stressful circumstances.

Review For Scott Serbin

Posted by FMDD User
November 03, 2022
He has always been accurate with her diagnoses and is aware of everything that is going on with your child. I totally recommend him!

Review For Scott Serbin

Posted by FMDD User
November 21, 2022
We believe he had spent enough time preparing to manage our child in the future. I strongly recommend him!!

Review For Scott Serbin

Conditions Treated
  • Torticollis
  • Lactose intolerance
  • Kidney infection
  • Stroke
  • Kawasaki disease
  • Irritable bowel syndrome
  • Melanoma
  • Insomnia
  • 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
  • Diabetes
  • Dermatitis
  • Depression
  • Deep vein thrombosis
  • Seizures
  • Cystic fibrosis
  • Congestive heart failure
  • Concussion
  • Chronic fatigue syndrome
  • 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
  • Allergies
  • 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
  • Digeorge syndrome
  • Dravet syndrome
  • Duchenne muscular dystrophy
  • Ebstein's anomaly
  • Ectodermal dysplasias
  • Encephalocele
  • Encopresis
  • Epicanthal folds
  • Epispadias
  • Erb's palsy
  • Esophageal atresia
  • Esotropia
  • Ewing sarcoma
  • Exercise induced asthma
  • Fanconi anemia
  • Food allergy
  • Fragile x syndrome
  • Galactosemia
  • Gastroschisis
  • Gingivostomatitis
  • Growth hormone deficiency
  • Head lice
  • Hemolytic uremic syndrome
  • Hemophilia a
  • Henoch schonlein purpura
  • Hermansky pudlak syndrome
  • Hirschsprung disease
  • Holoprosencephaly
  • Horseshoe kidney
  • Hydranencephaly
  • Hydrops fetalis
  • Hypophosphatasia
  • Hypoplastic left heart syndrome
  • Hypospadias
  • Hypotonia
  • Intussusception
  • Juvenile dermatomyositis
  • Juvenile idiopathic arthritis
  • Kabuki syndrome
  • Knock knees
  • Krabbe disease
  • Kwashiorkor
  • Langerhans cell histiocytosis
  • Laryngomalacia
  • Lazy eye
  • Legg calve perthes disease
  • Lennox gastaut syndrome
  • Lesch nyhan syndrome
  • Lissencephaly
  • Maple syrup urine disease
  • Microcephaly
  • Micrognathia
  • Microtia
  • Moebius syndrome
  • Mumps
  • Munchausen syndrome by proxy
  • Myelomeningocele
  • Necrotizing enterocolitis
  • Neonatal abstinence syndrome
  • Nephrotic syndrome
  • Neuroblastoma
  • Newborn jaundice
  • Noma
  • Noonan syndrome
  • Omphalocele
  • Osgood schlatter disease
  • Osteogenesis imperfecta
  • Otitis
  • Otitis media
  • Parainfluenza
  • Patent ductus arteriosus
  • Pectus carinatum
  • Pectus excavatum
  • Pertussis
  • Pfeiffer syndrome
  • Phenylketonuria
  • Pityriasis alba
  • Plagiocephaly
  • Poland syndrome
  • Polydactyly
  • Pompe disease
  • Precocious puberty
  • Progeria
  • Purpura
  • Rett syndrome
  • Reye syndrome
  • Rhabdomyosarcoma
  • Rheumatic fever
  • Rickets
  • Rubella
  • 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
  • Add adhd
  • Adenosine deaminase deficiency
  • Adrenoleukodystrophy
  • Aicardi goutieres syndrome
  • Aicardi syndrome
  • Albright's hereditary osteodystrophy
  • Alexander disease
  • 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
  • Congenital hyperinsulinism
  • Craniotabes
  • 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
  • Ring chromosome 18
  • 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 philtrum
  • 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
more..
Treatments & Procedures
  • Pediatric urgent care
  • Vaccines
  • Circumcision
  • Ear tubes
  • Well child visits
  • Immunization
  • Lumbar puncture
  • Pediatric laproscopy
  • Pediatric thoracoscopy
  • Medical ear piercing
  • Tetralogy of fallot repair
  • Tof repair
  • Pediatric sleep problems
  • Prematurity and low birth weight
Additional Services
  • Nutrition Coaching
  • LGBTQ Competent / Friendly
  • Travel Medicine

Frequently Asked Questions

Where is Pinnacle Pediatrics located?

Pinnacle Pediatrics is located in 1606 Twin Oaks Drive Sewickley, PA 15143 Sewickley, PA 15143.

What are the various modes of payment does Pinnacle Pediatrics Accept?

Pinnacle Pediatrics accepts Card | Cash.

What are the doctors who practice in Pinnacle Pediatrics specialize in?

Currently there are around 1 providers practice in Pinnacle Pediatrics who specialise in Concierge Pediatrics, etc

How can I make appointments with doctors in Pinnacle Pediatrics?

You can take appointments for doctors who practice in Pinnacle Pediatrics online on their website or by calling them.

Location