Shamaila Gill, MD
- Neonatologist, Assistant Professor at UT Southwestern Medical Center
- Languages spoken: English
- Locations (1)
Biography
Shamaila Gill, M.D., is a neonatologist at Children's Health and an Associate Professor at UT Southwestern.
Dr. Gill completed her medical education at Hamdard College of Medicine and Dentistry, Karachi Pakistan. She completed her pediatric residency at Texas Tech in Lubbock. She then obtained her Neonatal-Perinatal medicine training at University of Louisville.
Dr. Gill's clinical interests include long term neurodevelopmental outcomes of patients with prolonged and complicated stays in NICU, and the benefits of early childhood intervention in high risk patients.
Education and Training
- Medical School
- Hamdard College of Medicine and Dentistry (2003)
- Residency
- Texas Tech University Health Sciences Center (2013), Pediatrics
- Fellowship
- University of Louisville School of Medicine (2016), Neonatal-Perinatal Medicine
- Board Certification
- American Board of Pediatrics-Neonatal-Perinatal Medicine
- American Board of Pediatrics
Conditions Treated
- Pediatric lordosis (swayback)
- Anencephaly
- Anorectal malformation (imperforate anus or ARM)
- Bladder exstrophy
- Bladder outlet obstruction
- Bowel atresia
- Brachydactyly (symbrachydactyly)
- Cloacal exstrophy
- Colon atresia
- Congenital arteriovenous malformations
- Congenital diaphragmatic hernia (CDH)
- Congenital heart disease
- Congenital infections
- Congenital lung lesions
- Congenital pulmonary airway malformation (CPAM)
- Cystic fibrosis (CF) in children
- Down syndrome in children
- Encephalocele in children
- Esophageal atresia (EA)
- Gastroschisis
- Goldenhar syndrome (oculo-auriculo-vertebral dysplasia or OAV)
- Hirschsprung's disease
- Hydrops
- Hypoxic-ischemic encephalopathy (intrapartum asphyxia - HIE)
- Isolated craniosynostosis
- Jejunal and ileal atresia
- Low birth weight
- Meconium aspiration in newborns
- Muscular dystrophy (MD) in children
- Neonatal diabetes
- Newborn tumors
- Noonan syndrome (NS)
- Omphalocele
- Open neural tube defects (ONTDs)
- Osteogenesis imperfecta (OI)
- Pediatric abdominal masses
- Pediatric achondroplasia (dwarfism)
- Pediatric ambiguous genitalia
- Pediatric biliary atresia
- Pediatric chronic lung disease (CLD)
- Pediatric craniosynostosis
- Pediatric cytomegalovirus
- Pediatric duodenal atresia
- Pediatric edema
- Pediatric Ehlers-Danlos syndrome (EDS or elastic skin)
- Pediatric encephalopathy (encephalitis)
- Pediatric enteroviruses
- Pediatric feeding disorder
- Pediatric first unprovoked seizure
- Pediatric gastroesophageal reflux disease (GERD)
- Pediatric head and neck lumps
- Pediatric hemophilia
- Pediatric high blood pressure (hypertension)
- Pediatric hydrocephalus
- Pediatric hydronephrosis
- Pediatric hyperbilirubinemia (jaundice)
- Pediatric hypotonia
- Pediatric intestinal disorders
- Pediatric intraventricular hemorrhage and stroke
- Pediatric laryngomalacia
- Pediatric Low Blood Pressure (Hypotension)
- Pediatric mediastinal mass
- Pediatric metabolic diseases
- Pediatric necrotizing enterocolitis (NEC)
- Pediatric patent ductus arteriosus (PDA)
- Pediatric persistent pulmonary hypertension
- Pediatric pleural effusion
- Pediatric pyloric stenosis
- Pediatric respiratory distress syndrome (RDS)
- Pediatric rubella (German measles)
- Pediatric short bowel syndrome
- Pediatric syphilis
- Pediatric toxoplasmosis
- Pierre Robin syndrome
- Poland syndrome (Poland sequence)
- Prematurity
- Prenatal drug and alcohol exposure
- Pulmonary sequestration
- Renal malformation
- Retinopathy of prematurity (ROP)
- Sepsis and meningitis in children
- Skeletal dysplasias and abnormalities
- Spina bifida
- Syndromic craniosynostosis
- Tay-Sachs disease
- Tracheoesophageal fistula (TEF)
- VATER syndrome (VACTERL association)
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