Respiratory disorders in type-1 hereditary motor and sensory neuropathy

Type-1 hereditary motor and sensory neuropathy (HMSN I) is a slowly progressive disease resulting in distal muscle weakness with atrophy, and in sensory disturbance. Restrictive lung disease and respiratory muscle failure, common in many advanced neuromuscular disorders, is not a predominant feature...

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Veröffentlicht in:	Nihon Kyōbu Shikkan Gakkai zasshi 1996-08, Vol.34 (8), p.850-855
Hauptverfasser:	Akiba, Y, Kimura, T, Kitaoka, T, Toyoshima, E, Fujiuchi, S, Osanai, S, Nakano, H, Ohsaki, Y, Yahara, O, Kikuchi, K
Format:	Artikel
Sprache:	jpn
Schlagworte:	Charcot-Marie-Tooth Disease - complications Charcot-Marie-Tooth Disease - physiopathology Diaphragm - physiopathology Female Humans Male Middle Aged Neural Conduction Phrenic Nerve - physiopathology Respiration Disorders - etiology Respiration Disorders - physiopathology Sleep Apnea Syndromes - etiology Sleep Apnea Syndromes - physiopathology
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