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Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhood.
Muscle Nerve. 1981 Jan-Feb; 4(1):26-30.MN

Abstract

A detailed clinical and electrodiagnostic study has been undertaken of demyelinating polyneuropathy in 14 children (9 male, 5 female) from 11 sibships and their parents. The onset of symptoms was before the age of 2 years in 12 of the 14 children, and the condition in all cases was nonprogressive or very slowly progressive. In each case one of the parents had a slow motor nerve conduction velocity. Five of the 11 affected parents were completely asymptomatic. Electrodiagnostic studies in both parents of all children with demyelinating peripheral neuropathy are thus important to identify the dominantly inherited form of the disease.

Authors

No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

7231442

Citation

Vanasse, M, and V Dubowitz. "Dominantly Inherited Peroneal Muscular Atrophy (hereditary Motor and Sensory Neuropathy Type I) in Infancy and Childhood." Muscle & Nerve, vol. 4, no. 1, 1981, pp. 26-30.
Vanasse M, Dubowitz V. Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhood. Muscle Nerve. 1981;4(1):26-30.
Vanasse, M., & Dubowitz, V. (1981). Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhood. Muscle & Nerve, 4(1), 26-30.
Vanasse M, Dubowitz V. Dominantly Inherited Peroneal Muscular Atrophy (hereditary Motor and Sensory Neuropathy Type I) in Infancy and Childhood. Muscle Nerve. 1981 Jan-Feb;4(1):26-30. PubMed PMID: 7231442.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhood. AU - Vanasse,M, AU - Dubowitz,V, PY - 1981/1/1/pubmed PY - 1981/1/1/medline PY - 1981/1/1/entrez SP - 26 EP - 30 JF - Muscle & nerve JO - Muscle Nerve VL - 4 IS - 1 N2 - A detailed clinical and electrodiagnostic study has been undertaken of demyelinating polyneuropathy in 14 children (9 male, 5 female) from 11 sibships and their parents. The onset of symptoms was before the age of 2 years in 12 of the 14 children, and the condition in all cases was nonprogressive or very slowly progressive. In each case one of the parents had a slow motor nerve conduction velocity. Five of the 11 affected parents were completely asymptomatic. Electrodiagnostic studies in both parents of all children with demyelinating peripheral neuropathy are thus important to identify the dominantly inherited form of the disease. SN - 0148-639X UR - https://www.unboundmedicine.com/medline/citation/7231442/Dominantly_inherited_peroneal_muscular_atrophy__hereditary_motor_and_sensory_neuropathy_type_I__in_infancy_and_childhood_ L2 - https://doi.org/10.1002/mus.880040106 DB - PRIME DP - Unbound Medicine ER -