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Monomelic amyotrophy

Monomelic amyotrophy (MA) is a rare benign lower motor neuron disorder characterized by muscular weakness and wasting in the distal upper extremities during adolescence followed by a spontaneous halt in progression and a stabilization of symptoms.

Hemiatrophy

Undergrowth of the limbs that affects only one side.

Total: 1

(per page)

PMID (PMCID)
7774133	MALE	Adult
	[Electrodiagnosis of neuromuscular diseases--a syndrome of monomelic amyotrophy with spinal hemiatrophy, anti-GM1 antibodies and abnormal F-waves (MASH)].
	Kaji R. Rinsho Shinkeigaku. 1994;34(12):1272-5.
	[Electrodiagnosis of neuromuscular diseases--a syndrome of monomelic amyotrophy with spinal hemiatrophy, anti-GM1 antibodies and abnormal F-waves (MASH)].