clinic

Pediatric Surgery/UI Health

0 Stars (0 Review)

Pediatric Surgery/UI Health is a clinic that specializes in Concierge Pediatrics. The clinic is located in Chicago, Illinois. Pediatric Surgery/UI Health is known for housing expert physicians. Pediatric Surgery/UI Health offers all the services, treatments and procedures pertinent to the specialties mentioned above.

1 Doctor | Website
Overview
Providers
Reviews
Services
Location
About Pediatric Surgery/UI Health
Address

1801 W Taylor St Outpatient Care Center, Suite 3F, Chicago,
IL 60612

Modes of Payment

Card | Cash

Providers
Thom Lobe - 1801 W Taylor St, Chicago, IL 60612, USA, Chicago, Illinois, 60612
Thom Lobe, MD
Pediatric Surgery/UI Health
Concierge Pediatrics
(0)
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
1801 W Taylor St, Outpatient Care Center, Suite 3F, Chicago, IL 60612
Message
Call
Website
Reviews

No reviews found.

Conditions Treated
  • Torticollis
  • Lactose intolerance
  • Strep throat
  • 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
  • Hand-foot-and-mouth disease
  • Scurvy
  • Narcolepsy
  • Nausea
  • Generalized anxiety disorder
  • Gallstones
  • Fifth disease
  • Tinea versicolor
  • Eczema
  • Osteomyelitis
  • Sepsis
  • Smallpox
  • Ear infection
  • Tourette syndrome
  • Diphtheria
  • Diabetes
  • Dermatitis
  • Depression
  • Deep vein thrombosis
  • Seizures
  • Cystic fibrosis
  • Croup
  • Congestive heart failure
  • Concussion
  • Chronic fatigue syndrome
  • Cerebral palsy
  • Ulcerative colitis
  • Cellulitis
  • Celiac disease
  • Umbilical hernia
  • Pityriasis rosea
  • Cardiomyopathy
  • Canker sore
  • Psoriasis
  • Back pain
  • Skin cancer
  • Pulmonary embolism
  • Autism spectrum disorder
  • Atopic dermatitis
  • Asthma
  • Asperger's syndrome
  • Rectal prolapse
  • Restless legs syndrome
  • Vitiligo
  • Rosacea
  • Roseola
  • Sarcoidosis
  • Adhd
  • Sjogren's syndrome
  • Scarlet fever
  • Liver disease
  • Strabismus
  • Lupus
  • 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

Frequently Asked Questions

Where is Pediatric Surgery/UI Health located?

Pediatric Surgery/UI Health is located in 1801 W Taylor St Outpatient Care Center, Suite 3F, Chicago, IL 60612.

What are the various modes of payment does Pediatric Surgery/UI Health Accept?

Pediatric Surgery/UI Health accepts Card | Cash.

What are the doctors who practice in Pediatric Surgery/UI Health specialize in?

Currently there are around 1 providers practice in Pediatric Surgery/UI Health who specialise in Concierge Pediatrics, etc

How can I make appointments with doctors in Pediatric Surgery/UI Health?

You can take appointments for doctors who practice in Pediatric Surgery/UI Health online on their website or by calling them.

Location