A family pedigree exhibiting features of both multiple endocrine neoplasia type 1 and McCune-Albright syndromes.

2.50
Hdl Handle:
http://hdl.handle.net/10541/96986
Title:
A family pedigree exhibiting features of both multiple endocrine neoplasia type 1 and McCune-Albright syndromes.
Authors:
O'Halloran, Domhnall J; Shalet, Stephen M
Abstract:
The multiple endocrine neoplasia (MEN) type 1 and McCune-Albright syndromes share many clinical and biochemical characteristics. This report documents for the first time the occurrence and natural history of the McCune-Albright syndrome in a female with a strong family history of MEN type 1. There may be a functional link between both of these conditions, and there is a need to look for G-protein mutations as a mechanism for disease in MEN type 1.
Affiliation:
Department of Endocrinology, Christie Hospital, Manchester, United Kingdom.
Citation:
A family pedigree exhibiting features of both multiple endocrine neoplasia type 1 and McCune-Albright syndromes. 1994, 78 (3):523-5 J. Clin. Endocrinol. Metab.
Journal:
The Journal of Clinical Endocrinology and Metabolism
Issue Date:
Mar-1994
URI:
http://hdl.handle.net/10541/96986
PubMed ID:
7907339
Type:
Article
Language:
en
ISSN:
0021-972X
Appears in Collections:
All Christie Publications

Full metadata record

DC FieldValue Language
dc.contributor.authorO'Halloran, Domhnall Jen
dc.contributor.authorShalet, Stephen Men
dc.date.accessioned2010-04-21T10:32:54Z-
dc.date.available2010-04-21T10:32:54Z-
dc.date.issued1994-03-
dc.identifier.citationA family pedigree exhibiting features of both multiple endocrine neoplasia type 1 and McCune-Albright syndromes. 1994, 78 (3):523-5 J. Clin. Endocrinol. Metab.en
dc.identifier.issn0021-972X-
dc.identifier.pmid7907339-
dc.identifier.urihttp://hdl.handle.net/10541/96986-
dc.description.abstractThe multiple endocrine neoplasia (MEN) type 1 and McCune-Albright syndromes share many clinical and biochemical characteristics. This report documents for the first time the occurrence and natural history of the McCune-Albright syndrome in a female with a strong family history of MEN type 1. There may be a functional link between both of these conditions, and there is a need to look for G-protein mutations as a mechanism for disease in MEN type 1.en
dc.language.isoenen
dc.subject.meshChild-
dc.subject.meshFemale-
dc.subject.meshFibrous Dysplasia, Polyostotic-
dc.subject.meshHumans-
dc.subject.meshMultiple Endocrine Neoplasia-
dc.subject.meshPedigree-
dc.titleA family pedigree exhibiting features of both multiple endocrine neoplasia type 1 and McCune-Albright syndromes.en
dc.typeArticleen
dc.contributor.departmentDepartment of Endocrinology, Christie Hospital, Manchester, United Kingdom.en
dc.identifier.journalThe Journal of Clinical Endocrinology and Metabolismen

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