Phenotypes for disease #05083 (BVVLS (Brown-Vialetto-Van Laere syndrome (BVVLS)))

5 entries on 1 page. Showing entries 1 - 5.
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0000280318 see paper; ... Brown-Vialetto-Van Laere syndrome BVVLS2 Familial, autosomal recessive - - - - - Johan den Dunnen 00386512
0000280319 see paper; ..., progressive sensorineural deafness, childhood amyotrophic lateral sclerosis Brown-Vialetto-Van Laere syndrome BVVLS2 Familial, autosomal recessive - - - - - Johan den Dunnen 00386513
0000280320 - Brown-Vialetto-Van Laere syndrome BVVLS2 Familial, autosomal recessive - - - - - Johan den Dunnen 00386514
0000357703 onset 14y with GI problem including dysphagia, nausea and weight loss; Sensorineural hearing loss; Hand tremor; Atrophy of thenar and hypothenar; Mild generalized muscle weakness; EMG-NCV: motor neuron disease. Brown-Vialetto-Van Laere syndrome - Unknown 15y - - - - Johan den Dunnen 00472908
0000364547 - Brown-Vialetto-Van Laere syndrome BVVLS2 Familial, autosomal recessive - - - - - Ali Zeki Bedir 00480027
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