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Iran J Allergy Asthma Immunol ; 5(1): 35-7, 2006 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17242503

RESUMO

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.


Assuntos
Diagnóstico Diferencial , Neuropatias Hereditárias Sensoriais e Autônomas/diagnóstico , Disfunção de Fagócito Bactericida/diagnóstico , Pré-Escolar , Neuropatias Hereditárias Sensoriais e Autônomas/patologia , Humanos , Masculino , Disfunção de Fagócito Bactericida/patologia
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