Document Detail


Congenital sensory neuropathy as a differential diagnosis for phagocytic immunodeficiency.
MedLine Citation:
PMID:  17242503     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
There are few reports about congenital indifference to pain or Hereditary and Sensory Autonomic Neuropathy (HSAN). Several investigations for pathophysiology of this syndrome have been performed and different classifications about it. In this report we present a case of HSAN type II with general absence of pain and self amputations and leprosy-like damage of extremities which was suspected to be phagocytic immunodeficiency due to past history of repeated ulcer and abscess formation.
Authors:
Mohammad Gharagozlou; Fariborz Zandieh; Parviz Tabatabaei; Gholamreza Zamani
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Iranian journal of allergy, asthma, and immunology     Volume:  5     ISSN:  1735-1502     ISO Abbreviation:  Iran J Allergy Asthma Immunol     Publication Date:  2006 Mar 
Date Detail:
Created Date:  2007-01-23     Completed Date:  2007-10-11     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101146178     Medline TA:  Iran J Allergy Asthma Immunol     Country:  Iran    
Other Details:
Languages:  eng     Pagination:  35-7     Citation Subset:  IM    
Affiliation:
Department of Immunology and Allergy, Children Hospital Medical Center, Tehran University of Medical Sciences, Tehran, Iran. gharagoz@tums.ac.ir
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MeSH Terms
Descriptor/Qualifier:
Child, Preschool
Diagnosis, Differential*
Hereditary Sensory and Autonomic Neuropathies / diagnosis*,  pathology
Humans
Male
Phagocyte Bactericidal Dysfunction / diagnosis*,  pathology

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