PMID: 4017282Jun 1, 1985

Dominantly inherited syndrome of microcephaly and congenital lymphedema

Clinical Genetics
A K Leung

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.

References

Nov 1, 1979·The Journal of Pediatrics·R H Haslam, D W Smith
Sep 1, 1973·The Journal of Pediatrics·P K Kleinman
Jun 1, 1983·Journal of Medical Genetics·M BaraitserA T Piesowicz
Apr 1, 1980·Annals of Neurology·J F SchwartzJ C Hoffman

Citations

Jul 1, 1994·American Journal of Medical Genetics·L GiuffrèA Albanese
Jul 1, 1994·Archives of Disease in Childhood·N B Wright, H M Carty
Mar 1, 1996·Clinical Genetics·I AkaboshiS Yoshioka
Aug 1, 1991·The Annals of Otology, Rhinology, and Laryngology·G Har-ElM H Weiss
Dec 1, 1989·American Journal of Medical Genetics·R C HennekamA A Tillemans
Nov 1, 1988·Journal of Medical Genetics·P MerlobS H Reisner
Jan 8, 1999·American Journal of Medical Genetics·S Strenge, U G Froster
Aug 1, 1992·American Journal of Medical Genetics·M Feingold, L Bartoshesky
Nov 1, 1994·American Journal of Medical Genetics·B AngleJ M Opitz
Jan 1, 1987·American Journal of Medical Genetics·P Meinecke
Jul 1, 1987·American Journal of Medical Genetics·J L TolmieJ M Connor
Jul 1, 1989·American Journal of Medical Genetics·E Bawle, M Horton

Related Concepts

Genetic Conditions, Dominant
Milroy Disease
Microlissencephaly
Genealogical Tree

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