نتایج جستجو برای: cmt1a

تعداد نتایج: 183  

Journal: :Oman medical journal 2016
Patrick Scott Zandre Bruwer Khalsa Al-Kharusi Douja Meftah Fathiya Al-Murshedi

Charcot-Marie-Tooth neuropathy type 4B1 (CMT4B1) disease is a rare subtype of CMT4 with reported association of facial weakness, vocal cord paresis, chest deformities, and claw hands. We report the unusual occurrence of optic neuritis and cervical cord schwannoma in a male individual with confirmed CMT4B1 disease. Sequencing of the MTMR2 gene revealed a novel nonsense homozygous mutation c.1768...

Journal: :Human molecular genetics 1996
V Ionasescu C Searby V C Sheffield T Roklina D Nishimura R Ionasescu

Clinical, electrophysiological and genetic linkage studies were performed on a large autosomal dominant family with Charcot-Marie-Tooth axonal neuropathy type 2 (CMT2) with 38 members of which 14 were affected. Onset of the disease was between 16 and 30 years of age with weakness and atrophy of the hands more severe than of the feet with slow progressive course in 12 patients. Deep tendon refle...

Journal: :Neurology 2009
J D England G S Gronseth G Franklin G T Carter L J Kinsella J A Cohen A K Asbury K Szigeti J R Lupski N Latov R A Lewis P A Low M A Fisher D N Herrmann J F Howard G Lauria R G Miller M Polydefkis A J Sumner

BACKGROUND Distal symmetric polyneuropathy (DSP) is the most common variety of neuropathy. Since the evaluation of this disorder is not standardized, the available literature was reviewed to provide evidence-based guidelines regarding the role of laboratory and genetic tests for the assessment of DSP. METHODS A literature review using MEDLINE, EMBASE, and Current Contents was performed to ide...

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