Congenital sensory neuropathy as a differential diagnosis for phagocytic immunodeficiency
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
Search on Google
Index:
IMEMR (Eastern Mediterranean)
Main subject:
Phagocyte Bactericidal Dysfunction
/
Hereditary Sensory and Autonomic Neuropathies
/
Diagnosis, Differential
Type of study:
Case report
Limits:
Humans
/
Male
Language:
English
Journal:
Iran. J. Allergy Asthma Immunol.
Year:
2006
Similar
MEDLINE
...
LILACS
LIS