Document Detail


Hypertrichosis cubiti.
MedLine Citation:
PMID:  2773989     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Hypertrichosis is an unusual but well-recognized genetic condition. Hypertrichosis may be generalized or limited to specific body areas, in which case it is usually not associated with other anomalies. Five previous cases of hypertrichosis cubiti have been reported, with short stature in 2 sibs being the only other associated abnormalities. We report on a child with hairy elbows, developmental delay, facial asymmetry, and delayed speech with normal parents. Our patient may represent severe expression of the hairy elbow syndrome or constitute a previously unrecognized syndrome.
Authors:
D B Flannery; S M Fink; G Francis; P A Gilman
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  American journal of medical genetics     Volume:  32     ISSN:  0148-7299     ISO Abbreviation:  Am. J. Med. Genet.     Publication Date:  1989 Apr 
Date Detail:
Created Date:  1989-09-27     Completed Date:  1989-09-27     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  7708900     Medline TA:  Am J Med Genet     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  482-3     Citation Subset:  IM    
Affiliation:
Department of Pediatrics, Medical College of Georgia, Augusta 30912.
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MeSH Terms
Descriptor/Qualifier:
Child, Preschool
Elbow / abnormalities*
Facial Bones / abnormalities
Female
Growth Disorders / genetics
Humans
Hypertrichosis / genetics*
Language Development Disorders / genetics
Syndrome

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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