| Moebius sequence and hypogonadotrophic hypogonadism. | |
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MedLine Citation:
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PMID: 14556256 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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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. |
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Authors:
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Juliet E Jennings; Colm Costigan; William Reardon |
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Publication Detail:
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Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
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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:
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Created Date: 2003-10-13 Completed Date: 2004-06-18 Revised Date: 2008-05-21 |
Medline Journal Info:
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Nlm Unique ID: 101235741 Medline TA: Am J Med Genet A Country: United States |
Other Details:
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Languages: eng Pagination: 107-10 Citation Subset: IM |
Copyright Information:
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Copyright 2003 Wiley-Liss, Inc. |
Affiliation:
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Our Lady's Hospital for Sick Children, National Centre for Medical Genetics, Crumlin, Dublin, Ireland. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Cranial Nerve Diseases
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diagnosis Gonadotropins, Pituitary / deficiency* Humans Hypogonadism / diagnosis* Infant Infant, Newborn Kallmann Syndrome / diagnosis Male Mobius Syndrome / diagnosis* |
| Chemical | |
Reg. No./Substance:
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0/Gonadotropins, Pituitary |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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