Phe 84 deletion of the PMP22 gene associated with hereditary motor and sensory neuropathy HMSN III with multiple cranial neuropathy: clinical, neurophysiological and magnetic resonance imaging findings.

TitlePhe 84 deletion of the PMP22 gene associated with hereditary motor and sensory neuropathy HMSN III with multiple cranial neuropathy: clinical, neurophysiological and magnetic resonance imaging findings.
Publication TypeJournal Article
Year of Publication2001
AuthorsYener GG, Guiochon-Mantel A, Obuz F, Baklan B, Oztürk V, Kovanlikaya I, Cakmur R, Genç A
JournalJ Neurol
Volume248
Issue3
Pagination193-6
Date Published2001 Mar
ISSN0340-5354
KeywordsAdult, Cranial Nerve Diseases, Hereditary Sensory and Motor Neuropathy, Humans, Magnetic Resonance Imaging, Male, Myelin Proteins, Phenylalanine, Sequence Deletion
Abstract

Hereditary motor and sensory neuropathy (HMSN) is a heterogeneous group of peripheral neuropathies which are diagnosed on the basis of clinical, electrophysiological and neuropathological findings. Among the hypertrophic demyelinating neuropathies, HMSN III is the most severe. It is often associated with de novo mutations in the genes encoding for peripheral myelin proteins. While peripheral nerve hypertrophy is an expected finding in HMSN III, cranial nerve hypertrophy is exceptional. Here we describe a mutation in the PMP22 gene in a 19-year-old man with infantile onset of sensory motor polyneuropathy without family history and multiple cranial nerve hypertrophy shown by cranial magnetic resonance imaging.

DOI10.1007/s004150170225
Alternate JournalJ Neurol
PubMed ID11355152
Related Institute: 
MRI Research Institute (MRIRI)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065