A second case of microcephaly, microphthalmia, ectrodactyly (split-foot) and prognathism (MMEP)
- 1 January 1996
- journal article
- case report
- Published by Wolters Kluwer Health in Clinical Dysmorphology
- Vol. 5 (1) , 77-79
- https://doi.org/10.1097/00019605-199601000-00012
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.Keywords
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