Congenital Insensitivity to Pain With Anhydrosis
- 1 November 1979
- journal article
- research article
- Published by American Medical Association (AMA) in American Journal of Diseases of Children
- Vol. 133 (11) , 1153-1155
- https://doi.org/10.1001/archpedi.1979.02130110061011
Abstract
• Congenital indifference to pain with anhydrosis (CIPA) is a well-defined entity among a group of sensory deficiency syndromes. Children with this genetic disease are insensitive to pain and temperature and do not sweat and suffer from psychomotor retardation. Self-inflicted trauma may be severe and lead to insoluble orthopedic problems. To date, 11 cases have been reported. We have reviewed the literature and are describing two girls with CIPA, born to consanguine Jewish parents of Moroccan origin. Immunoglobulin deficiency has been reported in CIPA but an immunologic investigation on one of our cases showed only an early and transient deficiency of IgA. The presence in the family of a brother with ataxia telangiectasia and complete absence of IgA would seem to be irrelevant and it seems probable that the parents are heterozygotic for two disparate autosomal recessive syndromes. (Am J Dis Child 133:1153-1155, 1979)This publication has 7 references indexed in Scilit:
- Faculty Opinions recommendation of Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations.Published by H1 Connect ,2007
- CONGENITAL SENSORY NEUROPATHY WITH ANHIDROSIS - CASE-REPORT1976
- A Syndrome of the Neural CrestArchives of Neurology, 1966
- Congenital familial sensory neuropathy with anhidrosisThe Journal of Pediatrics, 1966
- Congenital Insensitivity to Pain with AnhydrosisArchives of Neurology, 1963
- Congenital Absence of PainArchives of Dermatology, 1962