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A second case of microcephaly, microphthalmia, ectrodactyly (split-foot) and prognathism (MMEP)
1SA Clinical Genetics Service, Women's and Children's Hospital, North Adelaide, South Australia.
Clinical Dysmorphology
|January 1, 1996
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.