Dominantly inherited syndrome of microcephaly and congenital lymphedema
- 1 June 1985
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 27 (6), 611-612
- https://doi.org/10.1111/j.1399-0004.1985.tb02047.x
Abstract
A Chinese family is reported in which microcephaly and congenital lymphedema have been observed in at least 4 generations. This combination of symptoms can be presumed to represent a rare but well defined hereditary syndrome transmitted by an autosomal dominant gene.Keywords
This publication has 6 references indexed in Scilit:
- THE GENETICS AND SUB-CLASSIFICATION OF MICROCEPHALY*Journal of Intellectual Disability Research, 2008
- Microcephaly and intracranial calcification in two brothersJournal of Medical Genetics, 1983
- Hereditary spinal arachnoid cysts, distichiasis, and lymphedemaAnnals of Neurology, 1980
- Autosomal dominant microcephalyThe Journal of Pediatrics, 1979
- Fabry’s Disease with Familial Lymphedema of the Lower LimbsEuropean Neurology, 1979
- Congenital lymphedema and yellow nailsThe Journal of Pediatrics, 1973