Dr. Ayne Kimberly Iafolla MD
Neonatal-Perinatal Medicine Specialist | Neonatal-Perinatal Medicine
9901 Medical Center Dr Nicu Rockville MD, 20850About
Dr. Ayne Iafolla is a Neonatal-Perinatal Physician practicing in Rockville, MD. Dr. Iafolla cares for the critically ill newborn and premature infants. Neonatal-Perinatal Physicians treat conditions such as breathing disorders, birth defects, infections, and any other life-threatening medical problems. They coordinate with their young patients families and other physicians to determine appropriate treatment.
Education and Training
Univ of Pittsburgh Sch of Med, Pittsburgh Pa 1984
University of Pittsburgh School of Medicine 1985
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP- Neonatal-Perinatal Medicine
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Genetic heterogeneity in MCAD deficiency: frequency of K329E allele and identification of three additional mutant alleles.
- Unbalanced translocation 46,XY,-15,+der(22)t(15;22)(q13;q11)pat: case report and review of the literature.
- Low plasma citrulline concentrations during protein restriction in an unaffected infant at risk for ornithine transcarbamylase deficiency.
- VATER and hydrocephalus: distinct syndrome?
- Medium-chain acyl-coenzyme A dehydrogenase deficiency and sudden infant death.
- Prenatal diagnosis of metabolic disease.
- Citrate therapy in argininosuccinate lyase deficiency.
- Medium-chain acyl CoA dehydrogenase deficiency: Its relationship to SIDS and the impact on genetic counseling.
- Megalencephaly in the neonatal period as the initial manifestation of glutaric aciduria type I.
- Medicinal leeches in the postoperative care of bladder exstrophy.
- Medium-chain acyl-coenzyme A dehydrogenase deficiency: clinical course in 120 affected children.
- Familial infantile apnea and immature beta oxidation.
- Fryns syndrome survivors and neurologic outcome.
- A case of duplication of 13q32-->qter and deletion of 18p11.32-->pter with mild phenotype: Patau syndrome and duplications of 13q revisited.
- Hemangioma, supraumbilical midline raphé, and coarctation of the aorta with a right aortic arch: single causal entity?
Treatments
- Birth Defects
- Congenital Heart Disease
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