A new type of hereditary motor and sensory neuropathy linked to chromosome 3

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Population

23 patients in 8 families with hereditary motor and sensory neuropathy in Okinawa, Japan

Design

Case_series

Authors

Discussion

Hypothesis-generating for novel HMSN-P; leaves open gene identification, validation, and clinical translation.

Population

23 patients in 8 families with hereditary motor and sensory neuropathy (proximal dominant form) (HMSN-P) in Okinawa, Japan

Outcome

Clinical, pathological, and genetic characterization of HMSN-Psurrogate

Identifies a new clinical entity of hereditary motor and sensory neuropathy (HMSN-P) and maps its gene locus to chromosome 3p14.1-q13.

Takashima et al. (1997) studied this question.

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