Hereditary Motor and Sensory Neuropathy (HMSN)

J Gordon Millichap

doi:10.15844/pedneurbriefs-1-5-1

Hereditary Motor and Sensory Neuropathy (HMSN)

Pediatric Neurology Briefs

Volume 1 (1987): Issue 5

By: J Gordon Millichap

Open Access

|Oct 1987

Abstract

Thirteen affected males and 25 obligate or probable heterozygous females with X-linked HMSN are reported from the Depts Neurology and Pathology, Duke Univ Med Centr, Durham, NC and Dept Neurology, Univ of Pennsylvania, Philadelphia, PA.

References

Rozear MP Pericak-Vance MA Fischbeck K Stajich JM Gaskell PC Jr Krendel DA Hereditary motor and sensory neuropathy, X-linked: a half century follow-up Neurology 1987 Sep 37 9 1460 5 3476859 10.1212/WNL.37.9.1460
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Dyck PJ Oviatt KF Lambert EH Intensive evaluation of referred unclassified neuropathies yields improved diagnosis Ann Neurol 1981 Sep 10 3 222 6 7294727 10.1002/ana.410100304
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-1-5-1 | Journal eISSN: 2166-6482

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Language: English

Page range: 31 - 31

Published on: Oct 1, 1987

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Heterozygous Patients,

Hyporeflexia,

Pes Cavus

© 1987 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 1 (1987): Issue 5