| Okihiro syndrome: thenar hypoplasia and Duane anomaly in three generations. | |
| | |
MedLine Citation:
|
PMID: 8287186 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
|
We describe a family with five members in three generations affected by Duane anomaly, three of whom also have minor radial ray abnormalities. This appears to be inherited as an autosomal dominant condition and is probably the same condition as that described by Temtamy et al. in 1975 and Okihiro et al. in 1977. One member also has congenital clubbing of the fingers and toes. |
| | |
Authors:
|
A Collins; M Baraitser; M Pembrey |
Related Documents
:
|
8882056 - Liver involvement in familial granulomatous arthritis (blau syndrome). 1259686 - An operated case of holt-oram syndrome with autosomal dominant inheritance. 8737646 - A new case of klippel-trenaunay-weber (ktw) syndrome: evidence of autosomal dominant in... 17431906 - Novel syndrome of cataracts, retinitis pigmentosa, late onset deafness and sperm abnorm... 11565636 - Os trigonum syndrome. 1880886 - Ocular cicatricial pemphigoid occurring as a sequela of stevens-johnson syndrome. |
Publication Detail:
|
Type: Case Reports; Journal Article |
Journal Detail:
|
Title: Clinical dysmorphology Volume: 2 ISSN: 0962-8827 ISO Abbreviation: Clin. Dysmorphol. Publication Date: 1993 Jul |
Date Detail:
|
Created Date: 1994-02-18 Completed Date: 1994-02-18 Revised Date: 2004-11-17 |
Medline Journal Info:
|
Nlm Unique ID: 9207893 Medline TA: Clin Dysmorphol Country: ENGLAND |
Other Details:
|
Languages: eng Pagination: 237-40 Citation Subset: IM |
Affiliation:
|
Department of Clinical Genetics, Institute of Child Health, London, UK. |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
Adult Child, Preschool Eye Abnormalities / genetics* Female Hand Deformities, Congenital / genetics Humans Male Pedigree Syndrome Thumb / abnormalities* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: A third patient with median cleft upper lip, mental retardation and pugilistic facies (W syndrome): ...
Next Document: Radial ray defect and Robin sequence: a new syndrome?