Neurofibromatous neuropathy.

Abstract:

:Three cases of chronic distal sensorimotor neuropathy are described in patients with neurofibromatosis. One had type 2 or central neurofibromatosis with a chromosome 22 deletion; the precise form of the disease was not established in the other two. A striking clinical feature was a diffuse nodular enlargement of the peripheral nerves. Nerve biopsies from all three cases demonstrated the presence of neurofibromatous pathology. Neurofibromatous neuropathy constitutes a rare manifestation of neurofibromatosis, related to diffuse neurofibromatous changes in the peripheral nerves.

journal_name

Muscle Nerve

journal_title

Muscle & nerve

authors

Thomas PK,King RH,Chiang TR,Scaravilli F,Sharma AK,Downie AW

doi

10.1002/mus.880130202

subject

Has Abstract

pub_date

1990-02-01 00:00:00

pages

93-101

issue

2

eissn

0148-639X

issn

1097-4598

journal_volume

13

pub_type

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