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PMID: 11971098 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't

Giant axonal neuropathy (GAN): case report and two novel mutations in the gigaxonin gene.

Neurology ·Vol. 58 ·No. 8 ·2002-04-23 ·Pages 1273-6

Kuhlenbäumer G, Young P, Oberwittler C, Hünermund G, Schirmacher A, Domschke K, Ringelstein B, Stögbauer F

Abstract

Giant axonal neuropathy (GAN) is an autosomal recessive neurologic disorder clinically characterized by a severe polyneuropathy, CNS abnormalities, and characteristic tightly curled hair. Recently, mutations in the gigaxonin gene have been identified as the underlying genetic defect. The authors report two novel mutations confirming that GAN is caused by mutations in the gigaxonin gene and raise the question whether some mutations may cause a mild subclinical neuropathy.

MeSH Terms
Adolescent Amino Acid Sequence Axons/pathology Cytoskeletal Proteins/genetics DNA Mutational Analysis Electrophysiology Humans Male Molecular Sequence Data Pedigree Peripheral Nervous System Diseases/genetics Point Mutation/genetics
Chemicals
Cytoskeletal Proteins GAN protein, human
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Kuhlenbäumer G
Department of Neurology, University of Münster, Germany.
Young P
Oberwittler C
Hünermund G
Schirmacher A
Domschke K
Ringelstein B
Stögbauer F
Article Info
Journal
Neurology
Abbr.
Neurology
ISSN
0028-3878
Published
2002-04-23
Pages
1273-6
Language
English
Region
United States
NLM ID
0401060
Subset
IM
Databases
GENBANK
AF291673
OMIM
256850
Corrections
ErratumIn
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