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A Case of Severe Early-Onset Neuropathy Caused by a Compound Heterozygous Deletion of the PMP22 Gene: Clinical and Neurographic Aspects.
- Source :
-
Neuropediatrics [Neuropediatrics] 2020 Jun; Vol. 51 (3), pp. 173-177. Date of Electronic Publication: 2019 Nov 29. - Publication Year :
- 2020
-
Abstract
- Heterozygous deletions of the gene PMP22 are associated to hereditary neuropathy with liability to pressure palsies (HNPP), a demyelinating neuromuscular disease causing variable transitory focal muscles weakness. Deletions involving both copies of PMP22 cause more severe phenotypes, with early-onset neuropathy and impairment in motor development. We report a patient with a severe early-onset demyelinating neuropathy, caused by two different inherited deletions of PMP22 , whose parents had an HNPP. The patient showed neurological signs and delay in motor development but normal intellective abilities. A motor and sensitive conduction study showed severe signs of demyelination, suggestive for Dejerine Sottas Syndrome (DSS). The patient's father had a typical HNPP caused by a heterozygous 17p11.2 deletion, encompassing PMP22 . The patient's mother reported no neuropathic symptoms, but in a nerve conduction studies, parents and several relatives showed signs of sensory-motor deficit with focal slowing of conduction at common sites of entrapment. Quantitative analysis of PMP22 , performed in our patient by multiplex ligation-dependent probe amplification, revealed a compound heterozygous status with the same deletion of the father and a deletion of PMP22 exon 5, after proved to be inherited from the mother. Therefore, when we face an early-onset, severe form of neuropathy, we have to consider rare forms of hereditary neuropathy caused by homozygous or compound heterozygous mutations in PMP22 , even if parents are asymptomatic; an exhaustive family history and an electrodiagnostic study are essential to guide genetic tests and to make a diagnosis.<br />Competing Interests: None.<br /> (Georg Thieme Verlag KG Stuttgart · New York.)
- Subjects :
- Child, Preschool
Female
Gene Deletion
Humans
Neural Conduction physiology
Pedigree
Arthrogryposis diagnosis
Arthrogryposis genetics
Arthrogryposis physiopathology
Hereditary Sensory and Motor Neuropathy diagnosis
Hereditary Sensory and Motor Neuropathy genetics
Hereditary Sensory and Motor Neuropathy physiopathology
Myelin Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1439-1899
- Volume :
- 51
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Neuropediatrics
- Publication Type :
- Academic Journal
- Accession number :
- 31784971
- Full Text :
- https://doi.org/10.1055/s-0039-3400985