clinic

Willow Pediatrics and Lactation

5 Stars (21 Reviews)

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

2 Doctors | Website
Overview
Providers
Reviews
Services
Location
About Willow Pediatrics and Lactation

"Willow Pediatrics and Lactation is a concierge practice with expertise in integrative pediatrics and breastfeeding medicine. We care for newborns to young adults. Our personalized care is truly tailored to the needs of your family, replacing assembly-line medicine and one-size-fits all mentality. By perfectly blending old-fashioned values and service with the most modern medicine, we have created a pediatric practice like no other!"

Address

1430 West Fillmore Street Unit 1E, Chicago,
IL 60624

Modes of Payment

Card | Cash

Providers
Filters
Amber Price - 1430 West Fillmore Street, Chicago, Illinois, 60624
Amber Price, MD
Willow Pediatrics and Lactation
Concierge Pediatrics
(11)
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
1430 West Fillmore Street, Unit 1E, Chicago, IL 60624
Message
Call
Website
Krystal Revai - 1430 West Fillmore Street, Chicago, Illinois, 60624
Krystal Revai, MD, MHP
Willow Pediatrics and Lactation
Concierge Pediatrics
(10)
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
1430 West Fillmore Street, Suite 1E, Chicago, IL 60624
Message
Call
Website
Reviews
Posted by FMDD User
February 25, 2022
Dr. Price has been there for our family throughout our transition to parenthood, from conception to toddlerhood. Well worth the money!

Review For Amber Price

Posted by FMDD User
June 10, 2022
An absolutely AMAZING pedetrician, lactation consultant, and person!

Review For Amber Price

Posted by FMDD User
January 28, 2022
We once took our infant to the emergency room, and having Dr. Price speak up for us by getting in touch with the hospital directly and interacting with the doctors on our behalf made all the difference in the world.

Review For Amber Price

Posted by FMDD User
April 22, 2022
personal and attentive treatment. Worth it for the peace of mind.

Review For Amber Price

Conditions Treated
  • Congestive heart failure
  • Chronic fatigue syndrome
  • Digeorge syndrome
  • Ectodermal dysplasias
  • Encephalocele
  • Epicanthal folds
  • Epispadias
  • Esotropia
  • Exercise induced asthma
  • Galactosemia
  • Head lice
  • Henoch schonlein purpura
  • Horseshoe kidney
  • Liver disease
  • Hydrops fetalis
  • Hypophosphatasia
  • Hypospadias
  • Intussusception
  • Juvenile dermatomyositis
  • Juvenile idiopathic arthritis
  • Kabuki syndrome
  • Krabbe disease
  • Kwashiorkor
  • Lazy eye
  • Lesch nyhan syndrome
  • Maple syrup urine disease
  • Munchausen syndrome by proxy
  • Nephrotic syndrome
  • Pityriasis alba
  • Congenital heart disease
  • Ebstein's anomaly
  • Hypoplastic left heart syndrome
  • Noonan syndrome
  • Patent ductus arteriosus
  • Rheumatic fever
  • Tetralogy of fallot
  • Truncus arteriosus
  • Ventricular septal defects
  • Aphantasia
  • Apraxia
  • Cerebellar hypoplasia
  • Dandy walker syndrome
  • Dravet syndrome
  • Duchenne muscular dystrophy
  • Erb's palsy
  • Fragile x syndrome
  • Holoprosencephaly
  • Hydranencephaly
  • Hypotonia
  • Lennox gastaut syndrome
  • Lissencephaly
  • Microcephaly
  • Moebius syndrome
  • Myelomeningocele
  • Pompe disease
  • Rett syndrome
  • Spinal muscular atrophy
  • Sturge weber syndrome
  • Tuberous sclerosis
  • Acute flaccid myelitis
  • Adrenoleukodystrophy
  • Aicardi goutieres syndrome
  • Aicardi syndrome
  • Alexander disease
  • Encopresis
  • Esophageal atresia
  • Food allergy
  • Hirschsprung disease
  • Necrotizing enterocolitis
  • Blount disease
  • Caudal regression syndrome
  • Clubfoot
  • Knock knees
  • Legg calve perthes disease
  • Osgood schlatter disease
  • Osteogenesis imperfecta
  • Pectus carinatum
  • Pectus excavatum
  • Polydactyly
  • Syndactyly
  • Choanal atresia
  • Laryngomalacia
  • Microtia
  • Otitis
  • Otitis media
  • Acute otitis externa
  • Congenital adrenal hyperplasia
  • Growth hormone deficiency
  • Phenylketonuria
  • Precocious puberty
  • Rickets
  • Albright's hereditary osteodystrophy
  • Gingivostomatitis
  • Mumps
  • Noma
  • Parainfluenza
  • Pertussis
  • Rubella
  • Generalized anxiety disorder
  • Fanconi anemia
  • Hemolytic uremic syndrome
  • Hemophilia a
  • Hermansky pudlak syndrome
  • Purpura
  • Thalassemia
  • Ewing sarcoma
  • Langerhans cell histiocytosis
  • Dermatitis
  • Atopic dermatitis
  • Eczema
  • Allergies
  • Sepsis
  • Hiatal hernia
  • Nausea
  • Seizures
  • Sarcoidosis
  • Diabetes
  • Cardiomyopathy
  • Cystic fibrosis
  • Pneumonia
  • Inguinal hernia
  • Pulmonary embolism
  • Scleroderma
  • Tinea versicolor
  • Hemangioma
  • Asthma
  • Stroke
  • Back pain
  • Multiple sclerosis
  • Gallstones
  • Lupus
  • Skin cancer
  • Melanoma
  • Canker sore
  • Pityriasis rosea
  • Vitiligo
  • Ear infection
  • Swimmer's ear
  • Psoriasis
  • Rosacea
  • Concussion
  • Insomnia
  • Lactose intolerance
  • Celiac disease
  • Umbilical hernia
  • Deep vein thrombosis
  • Hydrocele
  • Rectal prolapse
  • Harlequin ichthyosis
  • Roseola
  • Depression
  • Irritable bowel syndrome
  • Ulcerative colitis
  • Cellulitis
  • Kawasaki disease
  • Diphtheria
  • Smallpox
  • Osteomyelitis
  • Measles
  • Meningitis
  • Molluscum contagiosum
  • Scurvy
  • Sjogren's syndrome
  • Narcolepsy
  • Strep throat
  • Kidney infection
  • Torticollis
  • Cerebral palsy
  • Restless legs syndrome
  • Strabismus
  • Milia
  • Testicular torsion
  • Hand-foot-and-mouth disease
  • Fifth disease
  • Tourette syndrome
  • Croup
  • Autism spectrum disorder
  • Asperger's syndrome
  • Scarlet fever
  • Upper respiratory infection
  • Adhd
  • Neuroblastoma
  • Newborn jaundice
  • Reye syndrome
  • Add adhd
  • Anencephaly
  • Apert syndrome
  • Beckwith wiedemann syndrome
  • Brachydactyly
  • Cafe au lait spots
  • Cornelia de lange syndrome
  • Cri du chat syndrome
  • Crouzon syndrome
  • Cystinosis
  • Micrognathia
  • Pfeiffer syndrome
  • Poland syndrome
  • Progeria
  • Sotos syndrome
  • Stickler syndrome
  • Tay sachs disease
  • Treacher collins syndrome
  • Aarskog syndrome
  • Adams oliver syndrome
  • Adenosine deaminase deficiency
  • Caput succedaneum
  • Congenital diaphragmatic hernia
  • Cystic hygroma
  • Birthmarks
  • Craniosynostosis
  • Gastroschisis
  • Neonatal abstinence syndrome
  • Omphalocele
  • Plagiocephaly
  • Rhabdomyosarcoma
  • Selective mutism
  • Stork bite
  • Sudden infant death syndrome
  • Temper tantrums
  • Uncombable hair syndrome
  • Undescended testicle
  • Wilms tumor
  • Abo incompatibility
  • Acrodermatitis enteropathica
  • Cutis marmorata telangiectatica congenita
  • Dystrophic epidermolysis bullosa
  • Epidermolysis bullosa simplex
  • Gianotti crosti syndrome
  • Giant congenital melanocytic nevus
  • Hypohidrotic ectodermal dysplasia
  • Hypomelanosis of ito
  • Incontinentia pigmenti
  • Linear nevus sebaceous syndrome
  • Mongolian blue spots
  • Neonatal herpes
  • Netherton syndrome
  • Scalded skin syndrome
  • Aec syndrome
  • Baller gerold syndrome
  • Bannayan riley ruvalcaba syndrome
  • Bartsocas papas syndrome
  • Giant congenital nevus
  • Infantile digital fibromatosis
  • Infantile myofibromatosis
  • Junctional epidermolysis bullosa
  • Kerion celsi
  • Kindler syndrome
  • Megalencephaly capillary malformation syndrome
  • Meier gorlin syndrome
  • Perianal streptococcal cellulitis
  • Pik3ca related overgrowth spectrum
  • Pili torti
  • Pilonidal sinus disease
  • Pityriasis lichenoides et varioliformis acuta
  • Rothmund thomson syndrome
  • Scalp ear nipple syndrome
  • Sjogren larsson syndrome
  • Beare stevenson cutis gyrata syndrome
  • Cockayne syndrome type 2
  • Congenital generalized fibromatosis
  • Congenital herpes simplex
  • Cranioectodermal dysplasia
  • Curry jones syndrome
  • Farber lipogranulomatosis
  • Filippi syndrome
  • Gorlin chaudhry moss syndrome
  • Hemangioma thrombocytopenia syndrome
  • Nonbullous congenital ichthyosiform erythroderma
  • Phacomatosis pigmentokeratotica
  • Phacomatosis pigmentovascularis
  • 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
  • Infectious mononucleosis
  • Arginase deficiency
  • Aspartylglucosaminuria
  • Beta ketothiolase deficiency
  • Idiopathic neutropenia
  • Lactate dehydrogenase deficiency
  • Secondary immunodeficiency
  • Beta mannosidosis
  • Cold induced sweating syndrome
  • Diffuse mesangial sclerosis
  • Ring chromosome 18
  • Short philtrum
  • Donnai barrow syndrome
  • Eec syndrome
  • Ellis van creveld syndrome
  • Emery dreifuss muscular dystrophy
  • Fanconi syndrome
  • Fetal hydantoin syndrome
  • Floating harbor syndrome
  • Foxg1 syndrome
  • Fraser syndrome
  • Freeman sheldon syndrome
  • Frontonasal dysplasia
  • Fumarase deficiency
  • Glucose 6 phosphate dehydrogenase deficiency
  • Glutaric acidemia type 1
  • Gm1 gangliosidosis
  • Hallermann streiff syndrome
  • Hemihyperplasia
  • Heterotaxy syndrome
  • Holt oram syndrome
  • Hypochondroplasia
  • Jacobsen syndrome
  • Koolen de vries syndrome
  • Lowe syndrome
  • Menkes disease
  • Menkes syndrome
  • Miller dieker syndrome
  • Miller syndrome
  • Muenke syndrome
  • Myotonia congenita
  • Nail patella syndrome
  • Nemaline myopathy
  • Nephronophthisis
  • Neuronal ceroid lipofuscinoses
  • Niemann pick disease
  • Pierre robin sequence
  • Pitt hopkins syndrome
  • Potocki lupski syndrome
  • Propionic acidemia
  • Roberts syndrome
  • Robinow syndrome
  • Rubinstein taybi syndrome
  • Saethre chotzen syndrome
  • Seckel syndrome
  • Single palmar crease
  • Sirenomelia
  • Smith lemli opitz syndrome
  • Smith magenis syndrome
  • Spondyloepiphyseal dysplasia
  • Tetrasomy x
  • Thanatophoric dysplasia
  • Triple x syndrome
  • Trisomy 14 mosaicism
  • Vacterl association
  • Von gierke disease
  • Wagr syndrome
  • Weaver syndrome
  • Wiedemann steiner syndrome
  • Zellweger syndrome
  • Acalvaria
  • Achondrogenesis
  • Acrodysostosis
  • Adenylosuccinate lyase deficiency
  • Allan herndon dudley syndrome
  • Alpers huttenlocher syndrome
  • Alpha mannosidosis
  • Andersen disease
  • Argininosuccinic aciduria
  • Arterial tortuosity syndrome
  • Asphyxiating thoracic dystrophy
  • Behr syndrome
  • Chromosome 22 duplication
  • Chromosome 8p deletion
  • Classic galactosemia
  • Dubowitz syndrome
  • 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
  • Gangliosidosis
  • Gaucher disease type 2
  • Gaucher disease type 3
  • Geleophysic dysplasia
  • Glutaric acidemia type 2
  • Hennekam syndrome
  • Holocarboxylase synthetase deficiency
  • Icf syndrome
  • Isovaleric acidemia
  • Jackson weiss syndrome
  • Johanson blizzard syndrome
  • Kaufman oculocerebrofacial syndrome
  • Kniest dysplasia
  • Knobloch syndrome
  • L1 syndrome
  • Lambdoid synostosis
  • Langer mesomelic dysplasia
  • Leri weill dyschondrosteosis
  • Mandibuloacral dysplasia
  • Marden walker syndrome
  • Marinesco sjogren syndrome
  • Marshall smith syndrome
  • Marshall syndrome
  • Mass phenotype
  • Mckusick kaufman syndrome
  • Meckel syndrome
  • Medium chain acyl coa dehydrogenase deficiency
  • Mosaic trisomy 7
  • Mosaic trisomy 8
  • Mosaic trisomy 9
  • Mucolipidosis type 4
  • Mucopolysaccharidosis type 1
  • Mucopolysaccharidosis type 2
  • Mucopolysaccharidosis type 3
  • Myhre syndrome
  • Nicolaides baraitser syndrome
  • Nijmegen breakage syndrome
  • Ohdo syndrome
  • Opitz g bbb syndrome
  • Pallister hall syndrome
  • Pallister killian mosaic syndrome
  • Peho syndrome
  • Pentasomy x
  • Perlman syndrome
  • Peters plus syndrome
  • Popliteal pterygium syndrome
  • Prekallikrein deficiency
  • Primary carnitine deficiency
  • Progressive myoclonic epilepsy
  • Pyridoxine deficiency
  • Pyruvate carboxylase deficiency
  • Rapadilino syndrome
  • Renpenning syndrome
  • Russell silver dwarfism
  • Schimke immuno osseous dysplasia
  • Schindler disease
  • Schinzel giedion syndrome
  • Schwartz jampel syndrome
  • Sea blue histiocytosis
  • Severe congenital neutropenia
  • Short chain acyl coa dehydrogenase deficiency
  • Short qt syndrome
  • Short syndrome
  • Sialidosis
  • Simpson golabi behmel syndrome
  • Smith kingsmore syndrome
  • Snyder robinson syndrome
  • Spinal muscular atrophy type 2
  • Spinal muscular atrophy type 3
  • Spondylocostal dysostosis
  • Spondyloepiphyseal dysplasia congenita
  • Stuve wiedemann syndrome
  • Temple syndrome
  • Tetra amelia syndrome
  • Tetrasomy 9p
  • Thrombocytopenia absent radius syndrome
  • Townes brocks syndrome
  • Trisomy 2 mosaicism
  • Van maldergem syndrome
  • Vici syndrome
  • Wiedemann rautenstrauch syndrome
  • Anophthalmia plus syndrome
  • Ballinger wallace syndrome
  • Benign familial neonatal seizures
  • Bowen conradi syndrome
  • C syndrome
  • Carey fineman ziter syndrome
  • Charlie m syndrome
  • Cln1 disease
  • Cln3 disease
  • Cln5 disease
  • Coloboma of eye lens
  • Congenital afibrinogenemia
  • Congenital aplastic anemia
  • Congenital fibrinogen deficiency
  • Congenital hemolytic anemia
  • Congenital lipoid adrenal hyperplasia
  • Congenital microcoria
  • Congenital plasminogen deficiency
  • Craniofacial deafness hand syndrome
  • Cytochrome p450 oxidoreductase deficiency
  • Dehydrated hereditary stomatocytosis
  • Desbuquois syndrome
  • Dihydropteridine reductase deficiency
  • Distal 18q deletion syndrome
  • Encephalocele anencephaly
  • Familial glucocorticoid deficiency
  • Familial hypopituitarism
  • Familial paroxysmal nonkinesigenic dyskinesia
  • Familial porencephaly
  • Fetal akinesia sequence
  • Fetal thalidomide syndrome
  • Fountain syndrome
  • Frank ter haar syndrome
  • Galactose epimerase deficiency
  • Gemss syndrome
  • Genetic epilepsy with febrile seizures plus
  • Genital dwarfism
  • Hardikar syndrome
  • Hemophilia a or b
  • Histidinemia
  • Homocystinuria due to mthfr deficiency
  • Hyperlysinemia
  • Hypochondrogenesis
  • Inborn amino acid metabolism disorder
  • Increased head circumference
  • 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
  • Ornithine translocase deficiency
  • Orofaciodigital syndrome 1
  • Orotic aciduria type 1
  • Overhydrated hereditary stomatocytosis
  • Pena shokeir syndrome type 2
  • Peroxisomal acyl coa oxidase deficiency
  • Pgm1 cdg
  • Phosphoglycerate kinase deficiency
  • Phosphoglycerate mutase deficiency
  • Pmm2 congenital disorder of glycosylation
  • Potassium aggravated myotonia
  • Toriello carey syndrome
  • 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
  • Nephrogenic diabetes insipidus
  • Newborn low blood sugar
  • Pituitary dwarfism
  • Short stature
  • Delayed growth
  • Neonatal hypothyroidism
  • Pediatric obesity
  • Pinealectomy
  • Puberty disorder
  • Childhood hypophosphatasia
  • Hereditary hypophosphatemic rickets
  • Infant hyperglycemia
  • Isolated growth hormone deficiency
  • Neonatal severe hyperparathyroidism
  • Transient neonatal diabetes mellitus
  • Hemimegalencephaly
  • Infant botulism
  • Juvenile myoclonic epilepsy
  • Landau kleffner syndrome
  • Myoclonic epilepsy
  • Periventricular leukomalacia
  • Polymicrogyria
  • Pontocerebellar hypoplasia
  • Porencephaly
  • Rasmussen encephalitis
  • Spinal muscular atrophy type 1
  • West syndrome
  • Acute cerebellar ataxia
  • Bilirubin encephalopathy
  • Congenital mirror movement disorder
  • Diencephalic syndrome
  • Door syndrome
  • Dopa responsive dystonia
  • Early infantile epileptic encephalopathy
  • Intraventricular hemorrhage of the newborn
  • Marcus gunn phenomenon
  • Opsoclonus myoclonus syndrome
  • Periventricular heterotopia
  • Post traumatic epilepsy
  • Primary amebic meningoencephalitis
  • Satoyoshi syndrome
  • Congenital fiber type disproportion
  • Congenital muscular dystrophy type 1a
  • Cytoplasmic body myopathy
  • Epilepsy with myoclonic atonic seizures
  • Horizontal gaze palsy with progressive scoliosis
  • Hydrocephalus due to congenital stenosis of aqueduct of sylvius
  • Infantile onset spinocerebellar ataxia
  • Oculocerebrocutaneous syndrome
  • Oppenheim dystonia
  • Cytomegalovirus infection
  • Meningococcemia
  • Neonatal conjunctivitis
  • Neonatal sepsis
  • Torch syndrome
  • Toxocariasis
  • Congenital cytomegalovirus
  • Cytomegalic inclusion disease
  • H influenzae meningitis
  • Visceral larva migrans
  • Congenital mumps
  • Cryptosporidium enteritis
  • Rubella or measles
  • Duodenal atresia
  • Hepatoblastoma
  • Imperforate anus
  • Infantile pyloric stenosis
  • Tracheoesophageal fistula
  • Childhood pancreatitis
  • Colonic atresia
  • Congenital hepatic fibrosis
  • Congenital sucrase isomaltase deficiency
  • Gastroesophageal reflux in infants
  • Intestinal pseudo obstruction
  • Neonatal hemochromatosis
  • Atresia of small intestine
  • Berdon syndrome
  • Congenital nonhemolytic jaundice
  • Omphalomesenteric cyst
  • Primary intestinal lymphangiectasia
  • Cyclic neutropenia
  • Hemolytic disease of the newborn
  • Hemophagocytic lymphohistiocytosis
  • Hereditary spherocytosis
  • Juvenile myelomonocytic leukemia
  • Platelet storage pool deficiency
  • Childhood acute myeloid leukemia
  • Ganglioneuroma
  • Rhabdoid tumor
  • Rhabdomyosarcoma embryonal
  • Congenital mesoblastic nephroma
  • Embryonal tumor with multilayered rosettes
  • Ganglioneuroblastoma
  • Pediatric brain tumors
  • Pleuropulmonary blastoma
  • Primitive neuroectodermal tumor
  • Kohler disease
  • Slipped capital femoral epiphysis
  • Sprengel deformity
  • Congenital radioulnar synostosis
  • Congenital contractures
  • Congenital femoral deficiency
  • Stereotypic movement disorder
  • Transient tic disorder
  • Peer relationships
  • Developmental expressive language disorder
  • Developmental reading disorder
  • Pfapa
  • Toxic synovitis
  • Juvenile temporal arteritis
  • Neonatal onset multisystem inflammatory disease
  • Eisenmenger syndrome
  • Grass allergy
  • Meconium aspiration syndrome
  • Newborn transient tachypnea
  • Pulmonary atresia
  • Tracheobronchomalacia
  • Acute bronchiolitis
  • Congenital central hypoventilation syndrome
  • Congenital tracheomalacia
  • Idiopathic pulmonary hemosiderosis
  • Infantile apnea
  • Lung agenesis
  • Congenital pulmonary lymphangiectasia
  • Cystic adenomatoid malformation of lung
  • Endocardial cushion defect
  • Interrupted aortic arch
  • Pulmonary valve stenosis
  • Supravalvular aortic stenosis
  • Total anomalous pulmonary venous return
  • Transposition of the great arteries
  • Tricuspid atresia
  • Aortopulmonary window
  • Congenital anomalies of the heart
  • Congenital heart block
  • Double outlet left ventricle
  • Endocardial fibroelastosis
  • Mitral atresia
  • Pediatric myocarditis
  • Pulmonary atresia with intact ventricular septum
  • Right ventricle hypoplasia
  • Sternal cleft
  • Subvalvular aortic stenosis
  • Anomalous left coronary artery from the pulmonary artery
  • Arterial calcification of infancy
  • Congenital mitral stenosis
  • Fetal edema
  • High blood pressure in infants
  • Partial atrioventricular canal
  • Pulmonary atresia with ventricular septal defect
  • Ear tag
  • Metopic ridge
  • Penoscrotal transposition
  • Arrhinia
  • Exstrophy epispadias complex
  • Palatopharyngeal incompetence
  • Enlarged adenoids
  • Evans syndrome
  • Exstrophy of the bladder
  • Hemophilia b
  • Laryngeal cleft
  • Meatal stenosis
  • Meningocele
  • Nasal flaring
  • Otitis media with effusion
  • Potter syndrome
  • Prune belly syndrome
  • Retinopathy of prematurity
  • Severe combined immunodeficiency
  • Small for gestational age
  • Sunken fontanelles
  • Twin to twin transfusion syndrome
  • Velopharyngeal insufficiency
  • Aural polyps
  • Congenital nephrotic syndrome
  • Duplication of urethra
  • Infant hearing loss
  • Newborn head molding
  • Newborn polycythemia
  • Paroxysmal cold hemoglobinuria
  • Premature infant
  • Tracheal agenesis
  • Transient erythroblastopenia of childhood
  • Visceromegaly
  • And breastfeeding
  • Asphyxia neonatorum
  • Childhood iron deficiency anemia
  • Childhood volvulus
  • Fetal and neonatal alloimmune thrombocytopenia
  • Hygroma cervical
  • Neonatal ovarian cyst
  • Paris trousseau thrombocytopenia
  • Hmpv virus
more..
Treatments & Procedures
  • Ear tubes
  • Lumbar puncture
  • Well child visits
  • Vaccines
  • Pediatric urgent care
  • Immunization
  • Circumcision
  • Medical ear piercing
  • Tetralogy of fallot repair
  • Tof repair
  • Prematurity and low birth weight
  • Pediatric laproscopy
  • Pediatric thoracoscopy
  • Pediatric sleep problems

Frequently Asked Questions

Where is Willow Pediatrics and Lactation located?

Willow Pediatrics and Lactation is located in 1430 West Fillmore Street Unit 1E, Chicago, IL 60624.

What are the various modes of payment does Willow Pediatrics and Lactation Accept?

Willow Pediatrics and Lactation accepts Card | Cash.

What are the doctors who practice in Willow Pediatrics and Lactation specialize in?

Currently there are around 2 providers practice in Willow Pediatrics and Lactation who specialise in Concierge Pediatrics, etc

How can I make appointments with doctors in Willow Pediatrics and Lactation?

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

Location
SALE! Lab Tests - No Doctor/Insurance needed. Order Now ✕