Document Detail


Multiple endocrine neoplasia 2 (MEN 2)/MEN 2A (Sipple syndrome).
MedLine Citation:
PMID:  7712656     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Multiple endocrine neoplasia type 2A (MEN 2A, Sipple syndrome) is an autosomal dominant phakomatosis and is most likely a paracrinopathy. The cardinal manifestations of MEN 2A--medullary thyroid carcinoma, pheochromocytoma, and hyperparathyroidism--indicate that the condition is one of the inherited cancer syndromes. Cutaneous, lichen amyloidosis-like lesions place MEN 2A among the genodermatoses. The gene of MEN 2A, designated as MEN2A, is in the pericentromeric region of chromosome 10; this allows for reliable prenatal and presymptomatic DNA diagnosis.
Authors:
B G Kousseff
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Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  Dermatologic clinics     Volume:  13     ISSN:  0733-8635     ISO Abbreviation:  Dermatol Clin     Publication Date:  1995 Jan 
Date Detail:
Created Date:  1995-05-12     Completed Date:  1995-05-12     Revised Date:  2005-11-16    
Medline Journal Info:
Nlm Unique ID:  8300886     Medline TA:  Dermatol Clin     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  91-7     Citation Subset:  IM    
Affiliation:
Division of Medical Genetics, University of South Florida, Tampa, USA.
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MeSH Terms
Descriptor/Qualifier:
Adrenal Gland Neoplasms / genetics,  pathology
Amyloidosis / genetics,  pathology
Carcinoma / genetics,  pathology
Chromosomes, Human, Pair 10 / genetics
Humans
Hyperparathyroidism / genetics,  pathology
Lichenoid Eruptions / genetics,  pathology
Multiple Endocrine Neoplasia Type 2a / genetics*,  pathology
Pheochromocytoma / genetics,  pathology
Skin Diseases / genetics,  pathology
Thyroid Neoplasms / genetics,  pathology

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


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