Document Detail


Hereditary Punctate Palmoplantar Keratoderma (PPK) (Brauer-Buschke-Fischer Syndrome).
MedLine Citation:
PMID:  15187307     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We describe the first case of a sixty-five-year-old male field worker from India, having lesions of hereditary punctate palmoplantar keratoderma with an autosomally dominant pattern of inheritance. Associations included nail abnormalities in the form of longitudinal ridging, onychorrhexis, onychoschizia, trachyonychia and notching, which has been reported only on one previous occasion. The article also presents a brief review of the literature.
Authors:
Ritika Gupta; Shilpa Mehta; Deepika Pandhi; Archana Singal
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Publication Detail:
Type:  Case Reports; Journal Article; Review    
Journal Detail:
Title:  The Journal of dermatology     Volume:  31     ISSN:  0385-2407     ISO Abbreviation:  J. Dermatol.     Publication Date:  2004 May 
Date Detail:
Created Date:  2004-06-09     Completed Date:  2004-07-02     Revised Date:  2005-11-16    
Medline Journal Info:
Nlm Unique ID:  7600545     Medline TA:  J Dermatol     Country:  Japan    
Other Details:
Languages:  eng     Pagination:  398-402     Citation Subset:  IM    
Affiliation:
Department of Dermatology & STD, University College of Medical Sciences and Guru Teg Bahadur Hospital, Delhi, India.
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MeSH Terms
Descriptor/Qualifier:
Aged
Diagnosis, Differential
Genetic Predisposition to Disease
Humans
Keratoderma, Palmoplantar / diagnosis*,  genetics
Male
Pedigree

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


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