Hereditary Neuropathy With Liability To Pressure Palsies

dc.contributor.author	Omar, Mohammed
dc.date.accessioned	2019-06-25T09:07:46Z
dc.date.available	2019-06-25T09:07:46Z
dc.date.issued	2019-03-04
dc.identifier.uri	http://repository.limu.edu.ly/handle/123456789/970
dc.description	The HNPP is rare disease caused by deletion on chromosome 17. -The symptoms occur in childhood period, the PMP22 gene mutation is the main cause of this condition by affected myelin sheath in peripheral nerves the main symptoms is numbness and pain in the affected nerves. -Surgical decompression of nerves is not beneficial and may cause harm, the PMP22 gene mutation can cause other conditions such as , the PMP22 gene mutation can cause other conditions such as : Charcot-Marie-Tooth disease, and Yuan-Harel-Lupski syndrome. -physical thereby also used to helps muscles function.	en_US
dc.language.iso	en	en_US
dc.publisher	faculty of Basic Medical Science - Libyan International Medical University	en_US
dc.rights	Attribution 3.0 United States	*
dc.rights.uri	http://creativecommons.org/licenses/by/3.0/us/	*
dc.title	Hereditary Neuropathy With Liability To Pressure Palsies	en_US
dc.type	Other	en_US

Except where otherwise noted, this item's license is described as Attribution 3.0 United States