The Lenz microphthalmia syndrome: A case report
- 1 January 1983
- journal article
- case report
- Published by Taylor & Francis in Ophthalmic Paediatrics and Genetics
- Vol. 3 (2) , 103-107
- https://doi.org/10.3109/13816818309007826
Abstract
The association of microphthalmia and/or anophthalmia with microcephaly, vertebral, renal, urogenital and congenital heart diseases, has been recognized by Lenz as a distinct syndrome with X-linked recessive inheritance. Four familial and two sporadic cases have been published. The author reports a new sporadic case.Keywords
This publication has 4 references indexed in Scilit:
- Linkage Studies in Lenz MicrophthalmiaHuman Heredity, 1975
- X-Linked Colobomatous Microphthalmos and other Congenital AnomaliesAmerican Journal of Ophthalmology, 1971
- Heredofamilial Bilateral AnophthalmiaArchives of Ophthalmology (1950), 1963
- Recessiv-geschlechtsgebundene Mikrophthalmie mit multiplen Mi bildungenEuropean Journal of Pediatrics, 1955