| Literature DB >> 7747769 |
C McElveen1, M V Carvajal, D Moscatello, J Towner, Y Lacassie.
Abstract
We report on an individual with severe mental retardation, seizures, microcephaly, unusual face, scoliosis, and cleft feet and cleft right hand. The chromosomal study showed a proximal interstitial deletion 7q (q11.23q22). From our review of the literature, 11 patients have been reported with ectrodactyly (split hand/split foot malformation) and proximal/intermediate interstitial deletions or rearrangements of 7q. The critical segment for ectrodactyly seems to be located between 7q21.2 and 7q22.1. This malformation is present in 41% of the patients whose deletion involves the critical segment.Entities:
Mesh:
Year: 1995 PMID: 7747769 DOI: 10.1002/ajmg.1320560102
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299