These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Search MEDLINE/PubMed
Title: [Recurrent palsies--consider hereditary pressure neuropathy!]. Author: Liedholm LJ. Journal: Lakartidningen; 1998 Apr 01; 95(14):1527-31. PubMed ID: 9564140. Abstract: Three cases of hereditary neuropathy with liability to pressure palsies (HNPP), characterised by the typical deletion in chromosome 17p11 2-12, are described in the article. The clinical manifestations were pain-free brachial plexus palsies in two patients (belonging to the same family), and multiple episodes of numbness and weakness in various nerves in the third patient. The clinical, electrophysiological, histological and genetic findings are reviewed.[Abstract] [Full Text] [Related] [New Search]