Julie Mirpuri-Hathiramani, MD
- Neonatologist, Associate Professor at UT Southwestern Medical Center
- Languages spoken: English
- Locations (1)
Biography
Julie Mirpuri-Hathiramani, M.D., is a neonatal-perinatal medicine specialist at Children's Health an an Associate Professor at UT Southwestern Medical Center.
Dr. Mirpuri-Hathiramani earned her medical degree at the University of Hong Kong. She completed her residency in pediatrics at Atlantic Health’s Goryeb Children’s Hospital in Morristown, New Jersey, followed by a fellowship in neonatal-perinatal medicine at Grady Memorial Hospital in Atlanta.
When she’s not at work, Dr. Mirpuri-Hathiramani enjoys reading, doing advocacy work, cooking, and watching all things “Star Wars.”
Education and Training
- Medical School
- University of Hong Kong (2000)
- Internship
- Hospital Authority of Hong Kong (2001), Rotating
- Residency
- Morristown Memorial Hospital (2007), Pediatrics
- Fellowship
- Grady Memorial Hospital - GME (2010), 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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