Document Detail

Familial pyoderma gangrenosum presenting in infancy.
MedLine Citation:
PMID:  8874107     Owner:  NLM     Status:  MEDLINE    
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.
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
Age of Onset
Child, Preschool
Inflammatory Bowel Diseases / complications
Pyoderma Gangrenosum* / complications,  diagnosis,  drug therapy,  genetics
Stomatitis / complications

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