Jessica Hartson Morse, MD
- Pediatrician - Newborn Medicine, Associate Professor at UT Southwestern Medical Center
- Languages spoken: English
- Locations (1)
Biography
Jessica Morse, M.D., is a neonatal-perinatal medicine physician at Children's Health and a Clinical Assoicate Professor at UT Southwestern Medical Center.
Dr. Morse earned her medical degree at the University of Texas Health Science Center Houston, and completed her residency at the UT Southwestern Residency Program in Austin. She is board certified in Pediatrics and is certified as a Neonatal Resuscitation Program Instructor.
Education and Training
- Medical School
- University of Texas Health Science Center at Houston (2011)
- Residency
- UT Southwestern Medical School - Austin (2014), Pediatrics
- 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)
- 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 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 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)
Departments and Programs
Locations
More Information
Research Interests
Professional Activities
