Document Detail


Familial pyoderma gangrenosum presenting in infancy.
MedLine Citation:
PMID:  8874107     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
CONCLUSION: This is the first reported family with PG affecting three siblings suggesting autosomal recessive inheritance. The diagnosis may be more difficult in infants due to absence of underlying associated disorders and the tendency of the lesions to appear in areas where infants frequently have other dermatoses. PG characteristically involves the buttocks, thighs and perianal area and spares the legs.
Authors:
H S al-Rimawi; F M Abuekteish; A S Daoud; M M Oboosi
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  European journal of pediatrics     Volume:  155     ISSN:  0340-6199     ISO Abbreviation:  Eur. J. Pediatr.     Publication Date:  1996 Sep 
Date Detail:
Created Date:  1997-01-16     Completed Date:  1997-01-16     Revised Date:  2014-07-29    
Medline Journal Info:
Nlm Unique ID:  7603873     Medline TA:  Eur J Pediatr     Country:  GERMANY    
Other Details:
Languages:  eng     Pagination:  759-62     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Age of Onset
Child
Child, Preschool
Female
Humans
Inflammatory Bowel Diseases / complications
Male
Pyoderma Gangrenosum* / complications,  diagnosis,  drug therapy,  genetics
Recurrence
Stomatitis / complications

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


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