hereditary motor and sensory neuropathy with acrodystrophy
Findings
No curated finding names hereditary motor and sensory neuropathy with acrodystrophy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A rare axonal hereditary motor and sensory neuropathy characterized by progressive axonal neuropathy with limb weakness and severe distal sensory loss in all limbs and acrodystrophic changes leading to painless non-healing ulcers, osteomyelitis, contractures and mutilating lesions with loss of terminal phalanges. One family with three affected siblings is described and there have been no further descriptions in the literature since 1999.
Definition from the Mondo Disease Ontology (MONDO:0019550), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
4 names
Resolves to: hereditary motor and sensory neuropathy with acrodystrophy
- Also called
- AR-CMT2 with acrodystrophyautosomal recessive axonal Charcot-Marie-Tooth disease with acrodystrophyautosomal recessive Charcot-Marie-Tooth type 2 with acrodystrophyHMSN with acrodystrophy