1.
Iranian Journal of Allergy, Asthma and Immunology. 2006; 5 (1): 35-37
in English
| IMEMR
| ID: emr-164205
ABSTRACT
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