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Eyby Leon, MD

Languages:
English, Spanish
Service: Genetics
Specialty/Profession:
Pediatric Genetics
Board Certifications:
Clinical Genetics/Clinical Biochemical Genetics
Areas of Clinical Interest:
Down syndrome, disorders of sex develpment
Education:
Undergraduate - Cayetano Heredia University (2004)
Internship - Harlem Hospital Center (2009)
Residency - Boston Medical Center (2010)
Fellowship - University of Utah Hospital (2012)
Clinic Locations: Fairfax
Keystone Publications:

Regier DS, Leon E, Counts DR, Tifft CJ, Zand DJ.  Concurrent diagnoses of Prader-Willi syndrome and GM2 gangliosidosis caused by uniparental disomy of chromosome 15.  Am J Med Genet A. 2015 Apr 21. 

Crippa BL, Leon E, Calhoun A, Lowichik A, Pasquali M, Longo N.  Biochemical abnormalities in Pearson syndrome.  Am J Med Genet A. 2015 Mar;167A(3):621-8.

Stittrich AB, Lehman A, Bodian DL, Ashworth J, Zong Z, Li H, Lam P, Khromykh A, Iyer RK, Vockley JG, Baveja R, Silva ES, Dixon J, Leon EL, Solomon BD, Glusman G, Niederhuber JE, Roach JC, Patel MS.  Mutations in NOTCH1 cause Adams-Oliver syndrome.  Am J Hum Genet. 2014 Sep 4;95(3):275-84.

Johnston JJ, Sapp JC, Curry C, Horton M, Leon E, Cusmano-Ozog K, Dobyns WB, Hudgins L, Zackai E, Biesecker LG.  Expansion of the TARP syndrome phenotype associated with de novo mutations and mosaicism.  Am J Med Genet A. 2014 Jan;164A(1):120-8.   

Service: Genetics