Document Detail


Moebius sequence and hypogonadotrophic hypogonadism.
MedLine Citation:
PMID:  14556256     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A distinct form of Moebius sequence is associated with hypogonadotrophic hypogonadism. There have been five such cases to date. We now add a further case with detailed neurologic, endocrine, and autopsy findings and offer a hypothesis drawing parallels with the already established basis of hypogonadotrophic hypogonadism in the X-linked form of Kallman syndrome.
Authors:
Juliet E Jennings; Colm Costigan; William Reardon
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Publication Detail:
Type:  Case Reports; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  American journal of medical genetics. Part A     Volume:  123A     ISSN:  1552-4825     ISO Abbreviation:  Am. J. Med. Genet. A     Publication Date:  2003 Nov 
Date Detail:
Created Date:  2003-10-13     Completed Date:  2004-06-18     Revised Date:  2008-05-21    
Medline Journal Info:
Nlm Unique ID:  101235741     Medline TA:  Am J Med Genet A     Country:  United States    
Other Details:
Languages:  eng     Pagination:  107-10     Citation Subset:  IM    
Copyright Information:
Copyright 2003 Wiley-Liss, Inc.
Affiliation:
Our Lady's Hospital for Sick Children, National Centre for Medical Genetics, Crumlin, Dublin, Ireland.
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MeSH Terms
Descriptor/Qualifier:
Cranial Nerve Diseases / diagnosis
Gonadotropins, Pituitary / deficiency*
Humans
Hypogonadism / diagnosis*
Infant
Infant, Newborn
Kallmann Syndrome / diagnosis
Male
Mobius Syndrome / diagnosis*
Chemical
Reg. No./Substance:
0/Gonadotropins, Pituitary

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


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