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Journal article

Clinical and genetic features of patients suffering from CMT4J

Abstract:

Mutations in the FIG4 gene have been identified in various diseases, including amyotrophic lateral sclerosis, Parkinson’s disease, and Charcot–Marie–Tooth 4 J (CMT4J), with a wide range of phenotypic manifestations. We present eight cases of CMT4J patients carrying the p.Ile41Thr mutation of FIG4. The patients were categorized according to their phenotype. Six patients had a pure CMT; whereas, two patients had a CMT associated with parkinsonism. Three patients had an early onset and exhibited more severe forms of the disease. Three others experienced symptoms in their teenage years and had milder forms. Two patients had a late onset in adulthood. Four patients showed electrophysiological evidence of conduction blocks, typically associated with acquired neuropathies. Consequently, two of them received intravenous immunoglobulin treatment without a significant objective response. Interestingly, two heterozygous patients with the same mutations exhibited contrasting phenotypes, one having a severe early-onset form and the other experiencing a slow disease progression starting at the age of 49. Notably, although 7 out of 8 patients in this study were compound heterozygous for the p.Ile41Thr mutation, only one individual was found to be homozygous for this genetic variant and exhibited an early-onset, severe form of the disease. Additionally, one patient who developed the disease in his youth was also diagnosed with hereditary neuropathy with pressure palsies. Our findings provide insights into the CMT4J subtype by reporting on eight heterogeneous patient cases and highlight the potential for misdiagnosis when conduction blocks or asymmetrical nerve conduction study results are observed in patients with FIG4 mutations.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1007/s00415-023-12076-4

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
Paediatrics
Oxford college:
Kellogg College
Role:
Author
ORCID:
0000-0001-9270-4061


Publisher:
Springer
Journal:
Journal of Neurology More from this journal
Volume:
271
Issue:
3
Pages:
1355-1365
Place of publication:
Germany
Publication date:
2023-11-11
Acceptance date:
2023-10-19
DOI:
EISSN:
1432-1459
ISSN:
0340-5354
Pmid:
37950760


Language:
English
Keywords:
Pubs id:
1564794
UUID:
uuid_5874d71a-e3fd-4b43-90e2-e4bb163299c5
Local pid:
pubs:1564794
Source identifiers:
W4388593005
Deposit date:
2025-12-11
ARK identifier:

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