Juvenile Muscular Atrophy of Unilateral Upper Extremity (Hirayama Disease)

Creators Tada Yukiko

Creators Fukusako Toshihiro

Creators Negoro Kiyoshi

Creators Nogaki Hiroshi

Creators Morimatsu Mitsunori

We have clinically examined 9 patients with juvenile muscular atrophy of unilateral upper extremity (Hirayama disease) , which is characterized by exclusive juvenile male occurrence, insudious onset, unilateral muscular atrophy of the hand and forearm, lack of definite sesory disturbances and non or very slow progressive course. Although the clinical features of our patients were basically consistent with those in previous reports, their ages at onset were slightly higher and cold paresis and fasciculation ossurred less frequently in our cases. Five patients were examined by cervical magnetic resonance imaging (MRI) at the anteflexed position in addition to the routine neutral position. As aresult, 4 were found to show both the spinal cord thinning and anterioi shifting of the dural sac at levels of C5-C7

[ISSN]0513-1812

[NCID]AA00594272