| Literature DB >> 10963103 |
A Polo1, R Aldegheri, L G Bongiovanni, T Cavallaro, N Rizzuto.
Abstract
We describe the case of a young girl suffering from thermoregulation disturbances, painless fractures and arthropathy since early childhood. The patient was diagnosed as having a hereditary sensory autonomic neuropathy. Although needle EMG, conventional nerve conduction studies and somatosensory evoked potentials gave normal results, sympathetic skin responses (SSRs) were absent. Sural nerve biopsy showed a substantial reduction in the number of small myelinated and unmyelinated fibers. We emphasize the importance of SSR testing in revealing a condition which is otherwise difficult to identify by electrophysiological techniques. The combined evidence of functional and morphological findings is strongly suggestive of selective peripheral nerve involvement.Entities:
Mesh:
Year: 2000 PMID: 10963103 DOI: 10.1055/s-2000-7488
Source DB: PubMed Journal: Neuropediatrics ISSN: 0174-304X Impact factor: 1.947