Document Detail


A case of Waardenburg syndrome and aganglionosis.
MedLine Citation:
PMID:  1440950     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Waardenburg's syndrome is characterized by a broad nasal root, pigmentation disturbance and congenital deafness while aganglionosis is described as the partial or complete lack of ganglion cells in the alimentary tract. This report describes a five-day-old male infant with Waardenburg's syndrome associated with total aganglionosis of the colon, ileum and distal jejunum and draws attention to the causal relationship between these two entities.
Authors:
E Aritürk; N Tosyali; N Aritürk
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  The Turkish journal of pediatrics     Volume:  34     ISSN:  0041-4301     ISO Abbreviation:  Turk. J. Pediatr.     Publication Date:    1992 Apr-Jun
Date Detail:
Created Date:  1992-12-17     Completed Date:  1992-12-17     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0417505     Medline TA:  Turk J Pediatr     Country:  TURKEY    
Other Details:
Languages:  eng     Pagination:  111-4     Citation Subset:  IM    
Affiliation:
Department of Pediatric Surgery, Dicle University Faculty of Medicine, Diyarbakir.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Hirschsprung Disease / complications*
Humans
Infant, Newborn
Male
Waardenburg's Syndrome / complications*

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


Previous Document:  The effect of nifedipine on secretory diarrhea in mice.
Next Document:  Kawasaki syndrome.