Dr. Neda Zadeh, Pediatric Genetics

At the forefront of genetics and genomics research and well-versed in the latest treatments, Dr. Neda Zadeh is dedicated to caring for patients with developmental disabilities, genetic disorders and birth defects. She has a strong interest in neurofibromatosis type 1 (NF1) and other neurocutaneous genetic conditions, muscular dystrophies, craniofacial disorders, and the genetics of autism. Dr. Zadeh has authored many abstracts, journal articles and book chapters.

Dr. Zadeh is a medical geneticist in the division of medical genetics at CHOC, director of the NF clinic at CHOC and the associate director of the Molecular Diagnostic Laboratory at Genetics Center. Dr. Zadeh joined the medical staff at CHOC after completing her internship and residency training in pediatrics at CHOC. She completed a fellowship in clinical genetics at Stanford University and a fellowship in clinical molecular genetics at UCLA. Dr. Zadeh received her medical degree from UCLA School of Medicine.

Dedicated to clinical excellence, Dr. Zadeh is board certified in clinical genetics, clinical molecular genetics and in pediatrics. She is a fellow of the American College of Medical Genetics and Genomics (ABMGG) and of the American Academy of Pediatrics (AAP).

Locations

CHOC Specialty Clinic
1201 W. La Veta Ave.
Orange, CA 92868
phone: 714-288-3500
fax: 714-288-3510

Genetics Center
211 S Main St
Orange, CA 92868

Education

• Medical School
  University of California, Los Angeles School of Medicine
• Internship and Residency – Pediatric
  CHOC Hospital, Orange, CA
• Fellowship – Clinical Genetics
  Stanford University, Stanford, CA
• Fellowship – Clinical Molecular Genetics
  University of California, Los Angeles, CA

Administrative Appointments

• Director, Molecular Diagnostic Laboratory, Genetics Center

Professional Organizations

• American College of Genetics and Genomics (ACMG)
• American Medical Association

Publications

Books and Chapters

Zadeh N, Hudgins L. Human Malformations and Related Anomalies. 3rd ed. Stevenson RE, Hall JG, Everman DR, Solomon BD, editors. New York: Oxford University Press; 2015. Chapter 3 and 4, Pectoral and Pelvic Girdles; Spine and Ribs1024p.

Zadeh N. Neonatology. 1 ed. Sunshine P, Stevenson D, Cohen R, editors. New York: McGraw-Hill Education/Medical; 2015. Common Dysmorphic Syndromes1408p.

Zadeh N. Duane’s Ophthalmology. 2013 Edition ed. Tasman W, Jaeger EA, editors. New York: LWW; 2013. The Phakomatoses.

Meeting Abstracts

Sutherland T, Zadeh N, Southern Reh C. Genetic findings in a subject with type 1 diabetes mellitus and congenital adrenal hyperplasia. Endocrine Society Meeting; 2015 March; San Diego, CA, USA. c 00 .

Zadeh N, Nicholls A, Kaplan LJ, Zadeh T. Patient with SMC1A partial gene deletion without facial features of Cornelia de Lange syndrome. David W. Smith Workshop on Malformations; 2013 September; Mont Tremblant, Quebec, Canada. c 00 .

Brennan M, Adam MP, Seaver LH, Myers A, Zadeh N, et al. Increased body mass during infancy and toddlerhood in Angelman syndrome patients with uniparental disomy and imprinting center changes. David W Smith Workshop on Malformations; 2012 September; c 00

Zadeh N, Zadeh T. Two patients with similar 8p23.1 deletions and differing phenotypes: case report and review of the medical literature. David W. Smith Workshop on Malformations; 2011 September; Los Angeles, CA, USA. c 00

Zadeh N, Casson-Parkin S, Lachman R, Manning M, Bernstein J. Variable expressivity of spondyloepiphyseal dysplasia tarda with progressive arthropathy (SEDT-PA) in a multiplex family.. David W Smith Workshop on Malformations; 2010; Union, WA, USA. c 00 .

Zadeh N, Zadeh T, Manning M. Abnormal methylation of LIT1 in female monozygotic twins discordant for Beckwith-Wiedemann syndrome. WSPR; 2010; Carmel, CA, USA. c 00

Zadeh N, Hudgins L, Norton ME. Nuchal translucency measurements in fetuses with spinal muscular atrophy. American College of Medical Genetics; 2010; Albuquerque, NM. c 00

Zadeh N, Sureka D, Slattery L, Hudgins L. Otocephaly and heterotaxy; possible mechanisms. David W. Smith Workshop on Malformations; 2009; Philadelphia, PA, USA. c 00 .

Zadeh N, Kwan A, Hudgins L. Morphological features in Netherton syndrome. WSPR; 2009; Carmel, CA, USA. c 00
Cusmano-Ozog K, Moore T, Niemi A, Zadeh N, Cowan T, et al. Evidence of redox imbalance in a patient with methylmalonic academy (mut0). SIMD; 2010; c 00 .

Bernstein J, Merker J, Zadeh N, Cherry A. Identification of a 2 MB deletion within 15q14 by oligonucleotide array CGH narrows the cleft palate critical region at this locus. American College of Medical Genetics; 2009; c 00