Document Detail


Familial atrophia maculosa varioliformis cutis: case report and pedigree analysis.
MedLine Citation:
PMID:  16181468     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Atrophia maculosa varioliformis cutis (AVMC) was first described in 1918, as a rarely reported form of idiopathic macular atrophy on the cheeks. Nineteen patients have been reported in the past 86 years. Recently we diagnosed a 25-year-old woman as AMVC and investigated her family history. We collected the clinical data of the pedigree and presumed that AVMV is in a autosomal dominant inheritance.
Authors:
T Qu; B Wang; K Fang
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  The British journal of dermatology     Volume:  153     ISSN:  0007-0963     ISO Abbreviation:  Br. J. Dermatol.     Publication Date:  2005 Oct 
Date Detail:
Created Date:  2005-09-26     Completed Date:  2006-01-12     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0004041     Medline TA:  Br J Dermatol     Country:  England    
Other Details:
Languages:  eng     Pagination:  821-4     Citation Subset:  IM    
Affiliation:
Department of Dermatology, Peking Union Medical College Hospital, Chinese Academy of Medical Science, Beijing 100730, China.
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Adult
Age of Onset
Atrophy / genetics,  pathology
Elastic Tissue / pathology
Facial Dermatoses / genetics,  pathology*
Female
Humans
Male
Pedigree
Skin / pathology*
Skin Diseases, Genetic / genetics,  pathology*

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


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