HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

A second case of microcephaly, microphthalmia, ectrodactyly (split-foot) and prognathism (MMEP).

Abstract
In 1993, Viljoen and Smart described a woman with ectrodactyly of the feet, midline facial cleft, microphthalmia, and mental retardation in association with a de novo chromosome 6;13 translocation. We present a man with similar features who had a normal karyotype.
AuthorsG Suthers, L Morris
JournalClinical dysmorphology (Clin Dysmorphol) Vol. 5 Issue 1 Pg. 77-9 (Jan 1996) ISSN: 0962-8827 [Print] England
PMID8867664 (Publication Type: Case Reports, Journal Article)
Topics
  • Adult
  • Foot Deformities, Congenital (pathology)
  • Humans
  • Male
  • Microcephaly (pathology)
  • Microphthalmos (pathology)
  • Prognathism (pathology)
  • Syndrome

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: