A family pedigree exhibiting features of both multiple endocrine neoplasia type 1 and McCune-Albright syndromes.
| dc.contributor.author | O'Halloran, Domhnall J | |
| dc.contributor.author | Shalet, Stephen M | |
| dc.date.accessioned | 2010-04-21T10:32:54Z | |
| dc.date.available | 2010-04-21T10:32:54Z | |
| dc.date.issued | 1994-03 | |
| dc.identifier.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. | en |
| dc.identifier.issn | 0021-972X | |
| dc.identifier.pmid | 7907339 | |
| dc.identifier.uri | http://hdl.handle.net/10541/96986 | |
| dc.description.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. | |
| dc.language.iso | en | en |
| dc.subject.mesh | Child | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | Fibrous Dysplasia, Polyostotic | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Multiple Endocrine Neoplasia | |
| dc.subject.mesh | Pedigree | |
| dc.title | A family pedigree exhibiting features of both multiple endocrine neoplasia type 1 and McCune-Albright syndromes. | en |
| dc.type | Article | en |
| dc.contributor.department | Department of Endocrinology, Christie Hospital, Manchester, United Kingdom. | en |
| dc.identifier.journal | The Journal of Clinical Endocrinology and Metabolism | en |
| html.description.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. |