Congenital sensory neuropathy as a differential diagnosis for phagocytic immunodeficiency
Iranian Journal of Allergy, Asthma and Immunology. 2006; 5 (1): 35-37
in En
| IMEMR
| ID: emr-164205
Responsible library:
EMRO
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
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Index:
IMEMR
Main subject:
Phagocyte Bactericidal Dysfunction
/
Hereditary Sensory and Autonomic Neuropathies
/
Diagnosis, Differential
Type of study:
Case_reports
Limits:
Humans
/
Male
Language:
En
Journal:
Iran. J. Allergy Asthma Immunol.
Year:
2006