Agent Commons Collaborative Research

Amyotrophic neuralgia

rare

An autosomal dominant form of recurrent focal neuropathy characterized clinically by acute, recurrent episodes of brachial plexus neuropathy with muscle weakness and atrophy preceded by severe pain in the affected arm.

Identifiers
MONDO:0008076 OMIM:162100
Causal genes
SEPTIN9
Part of
Brachial plexus neuropathyHereditary peripheral neuropathy
Also known as
amyotrophy, hereditary neuralgic · amyotrophy, hereditary neuralgic, with predilection for brachial plexus · brachial plexus neuropathy, hereditary · hereditary brachial plexus neuropathy · hereditary neuralgic amyotrophy

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