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PMID: 24878229 Published · ppublish English Case Reports Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Whole exome sequencing identifies three recessive FIG4 mutations in an apparently dominant pedigree with Charcot-Marie-Tooth disease.

Neuromuscular disorders : NMD ·Vol. 24 ·No. 8 ·2014-08-00 ·Pages 666-70

Menezes MP, Waddell L, Lenk GM, Kaur S, MacArthur DG, Meisler MH, Clarke NF

Abstract

Charcot-Marie-Tooth disease (CMT) is genetically heterogeneous and classification based on motor nerve conduction velocity and inheritance is used to direct genetic testing. With the less common genetic forms of CMT, identifying the causative genetic mutation by Sanger sequencing of individual genes can be time-consuming and costly. Next-generation sequencing technologies show promise for clinical testing in diseases where a similar phenotype is caused by different genes. We report the unusual occurrence of CMT4J, caused by mutations in FIG4, in a apparently dominant pedigree. The affected proband and her mother exhibit different disease severities associated with different combinations of compound heterozygous FIG4 mutations, identified by whole exome sequencing. The proband was also shown to carry a de novo nonsense mutation in the dystrophin gene, which may contribute to her more severe phenotype. This study is a cautionary reminder that in families with two generations affected, explanations other than dominant inheritance are possible, such as recessive inheritance due to three mutations segregating in the family. It also emphasises the advantages of next-generation sequencing approaches that screen multiple CMT genes at once for patients in whom the common genes have been excluded.

Keywords
Autosomal recessive CMT CMT4J Charcot–Marie–Tooth FIG4 Whole exome sequencing
MeSH Terms
Adolescent Adult Charcot-Marie-Tooth Disease/genetics,physiopathology Codon, Nonsense Dystrophin/genetics Family Female Flavoproteins/genetics Genes, Recessive Heterozygote Humans Pedigree Phosphoric Monoester Hydrolases/genetics Severity of Illness Index
Chemicals
Codon, Nonsense Dystrophin Flavoproteins FIG4 protein, human Phosphoric Monoester Hydrolases
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Menezes Manoj P
Institute for Neuroscience and Muscle Research, The Children's Hospital at Westmead, Sydney, Australia; Discipline of Paediatrics and Child Health, The University of Sydney, Sydney, Australia. Electronic address: manoj.menezes@health.nsw.gov.au.
Waddell Leigh
Institute for Neuroscience and Muscle Research, The Children's Hospital at Westmead, Sydney, Australia; Discipline of Paediatrics and Child Health, The University of Sydney, Sydney, Australia.
Lenk Guy M
Department of Human Genetics, University of Michigan, Ann Arbor, MI, USA.
Kaur Simranpreet
Institute for Neuroscience and Muscle Research, The Children's Hospital at Westmead, Sydney, Australia.
MacArthur Daniel G
Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA; Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA, USA; Department of Medicine, Harvard Medical School, Boston, MA, USA.
Meisler Miriam H
Department of Human Genetics, University of Michigan, Ann Arbor, MI, USA.
Clarke Nigel F
Institute for Neuroscience and Muscle Research, The Children's Hospital at Westmead, Sydney, Australia; Discipline of Paediatrics and Child Health, The University of Sydney, Sydney, Australia.
Supplementary Concepts
Charcot-Marie-Tooth Disease, Type 4j (Disease)
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Article Info
Journal
Neuromuscular disorders : NMD
Abbr.
Neuromuscul Disord
ISSN
1873-2364
Published
2014-08-00
Epub
2014-00-04
Pages
666-70
Language
English
Region
England
NLM ID
9111470
PMCID
PMC4096049
Subset
IM
Grants
NIGMS NIH HHS · R01 GM024872 · United States
NIGMS NIH HHS · R01 GM24872 · United States
Corrections
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