Literature DB >> 19922122

Madras motor neuron disease in Turkey.

Baris Isak1, Kayihan Uluc, Tulin Tanridag, Selda Ozsahin, Reinhard Dengler, Onder Us, Susanne Petri.   

Abstract

We present a 19-year-old female patient complaining of hoarseness and eyelid drooping. The neurological examination and laboratory investigations including genetic, radiological and electrophysiological evaluations were consistent with a juvenile-onset, predominantly bulbar, motor neuron disease with sensorineural hearing loss. The syndrome fulfilled the diagnostic criteria of Madras Motor Neuron Disease (MMND). Very few cases with MMND have been reported to date, and the majority are from south-eastern Asia. This is the first case reported from Turkey and indicates that the disease is not only regional but may also occur on the basis of rare de novo mutations.

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Year:  2009        PMID: 19922122     DOI: 10.3109/17482960802645016

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler        ISSN: 1471-180X


  1 in total

1.  A Madras Motor Neuron Disease Patient With Cerebellar Atrophy: A New Clinical Feature.

Authors:  Ling Long; Xiaodong Cai; Jia Liu; Zhuang Kang; Jing Li; Zizhen Huang; Ruomi Guo; Yan Zou; Zhengqi Lu
Journal:  Front Neurosci       Date:  2018-10-08       Impact factor: 4.677

  1 in total

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