Τετάρτη 18 Ιανουαρίου 2017

'This diagnosis can be extremely scary'.

'This diagnosis can be extremely scary'.

Nurs Stand. 2017 Jan 18;31(21):22-24

Authors: Newton-Snow T

Abstract
Neurofibromatosis type 2 (NF2) is a rare genetic disorder that occurs in an estimated one in 35,000 people. The condition is often life-limiting and involves tumours growing on the nervous system, typically on the hearing nerves, brain and spine. While the tumours are mainly benign, they can lead to hearing loss, deafness and problems with balance and mobility. Most patients will need surgery or other treatments for NF2-related brain or spinal cord tumours at some point in their lives.

PMID: 28097979 [PubMed - in process]



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