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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