Document Detail


Two brothers with keratosis follicularis spinulosa decalvans.
MedLine Citation:
PMID:  12399750     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Keratosis follicularis spinulosa decalvans is a rare, X-linked disorder affecting both the skin and eyes. There are few reports about this entity. The aim of this report is to describe 2 brothers with progressive scarring alopecia of the scalp, hypotrichosis with follicular prominence of the eyelashes, and extensive keratosis pilaris. The second patient has Down syndrome with palmoplantar keratoderma and partial alopecia of the eyebrows. We also reviewed the literature about this uncommon entity.
Authors:
Abdullah Alfadley; Khalid Al Hawsawi; Bo Hainau; Khalid Al Aboud
Publication Detail:
Type:  Case Reports; Journal Article; Review    
Journal Detail:
Title:  Journal of the American Academy of Dermatology     Volume:  47     ISSN:  0190-9622     ISO Abbreviation:  J. Am. Acad. Dermatol.     Publication Date:  2002 Nov 
Date Detail:
Created Date:  2002-10-25     Completed Date:  2002-11-19     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  7907132     Medline TA:  J Am Acad Dermatol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  S275-8     Citation Subset:  IM    
Affiliation:
Department of Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Alopecia / genetics
Child
Darier Disease / genetics*
Down Syndrome / genetics
Genetic Diseases, X-Linked / genetics
Humans
Keratoderma, Palmoplantar / genetics
Male

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


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