Expanding the spectrum of clinical and genetic characteristics of distal arthrogryposis type 5 caused by heterozygous variants in the PIEZO2 gene

Pathogenic heterozygous variants in the PIEZO2 gene cause distal arthrogryposis type 5 – a rare autosomal dominant disease, which is characterized by the development of congenital contractures, ophthalmoparesis, ptosis and restrictive respiratory disorders. We have presented clinical and genetic cha...

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Main Authors: E. L. Dadali, T. V. Markova, E. A. Melnik, S. S. Nikitin, I. V. Sharkova, O. V. Khalanskaya, L. A. Bessonov, E. A. Shestopalova, O. P. Ryzhkova, S. I. Trofimova, O. E. Agranovich, S. I. Kutsev
Format: Article
Language:Russian
Published: ABV-press 2024-05-01
Series:Нервно-мышечные болезни
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Online Access:https://nmb.abvpress.ru/jour/article/view/600
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author E. L. Dadali
T. V. Markova
E. A. Melnik
S. S. Nikitin
I. V. Sharkova
O. V. Khalanskaya
L. A. Bessonov
E. A. Shestopalova
O. P. Ryzhkova
S. I. Trofimova
O. E. Agranovich
S. I. Kutsev
author_facet E. L. Dadali
T. V. Markova
E. A. Melnik
S. S. Nikitin
I. V. Sharkova
O. V. Khalanskaya
L. A. Bessonov
E. A. Shestopalova
O. P. Ryzhkova
S. I. Trofimova
O. E. Agranovich
S. I. Kutsev
author_sort E. L. Dadali
collection DOAJ
description Pathogenic heterozygous variants in the PIEZO2 gene cause distal arthrogryposis type 5 – a rare autosomal dominant disease, which is characterized by the development of congenital contractures, ophthalmoparesis, ptosis and restrictive respiratory disorders. We have presented clinical and genetic characteristics of seven Russian patients with distal arthrogryposis type 5  caused by previously described and newly identified nucleotide variants in the PIEZO2 gene. It was shown that the most severe clinical manifestations were found in patients with newly identified nucleotide variants c.8238G>A (p.Trp274Ter) and c.7095G>T (p.Trp2365Cys), while in patients with other previously described variants c.8181_8183delAGA (p.Glu2727del) and c.2134A>G (p.Met712Val) the clinical phenotype is more moderately expressed. The dynamics of phenotype formation were also noted. It has been shown that the disease progression may occur as the child grows and requires monitoring of this group of patients.
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record_format Article
series Нервно-мышечные болезни
spelling doaj-art-38ae51ab9cb549f18d5c8a123744b86d2025-08-20T03:37:51ZrusABV-pressНервно-мышечные болезни2222-87212413-04432024-05-0114210.17650/2222-8721-2024-14-2-25-37380Expanding the spectrum of clinical and genetic characteristics of distal arthrogryposis type 5 caused by heterozygous variants in the PIEZO2 geneE. L. Dadali0T. V. Markova1E. A. Melnik2S. S. Nikitin3I. V. Sharkova4O. V. Khalanskaya5L. A. Bessonov6E. A. Shestopalova7O. P. Ryzhkova8S. I. Trofimova9O. E. Agranovich10S. I. Kutsev11Research Centre for Medical GeneticsResearch Centre for Medical GeneticsResearch Centre for Medical GeneticsResearch Centre for Medical GeneticsResearch Centre for Medical GeneticsResearch Centre for Medical GeneticsResearch Centre for Medical GeneticsResearch Centre for Medical GeneticsResearch Centre for Medical GeneticsH. Turner National Medical Research Center for Children’s Orthopedics and Trauma SurgeryH. Turner National Medical Research Center for Children’s Orthopedics and Trauma SurgeryResearch Centre for Medical GeneticsPathogenic heterozygous variants in the PIEZO2 gene cause distal arthrogryposis type 5 – a rare autosomal dominant disease, which is characterized by the development of congenital contractures, ophthalmoparesis, ptosis and restrictive respiratory disorders. We have presented clinical and genetic characteristics of seven Russian patients with distal arthrogryposis type 5  caused by previously described and newly identified nucleotide variants in the PIEZO2 gene. It was shown that the most severe clinical manifestations were found in patients with newly identified nucleotide variants c.8238G>A (p.Trp274Ter) and c.7095G>T (p.Trp2365Cys), while in patients with other previously described variants c.8181_8183delAGA (p.Glu2727del) and c.2134A>G (p.Met712Val) the clinical phenotype is more moderately expressed. The dynamics of phenotype formation were also noted. It has been shown that the disease progression may occur as the child grows and requires monitoring of this group of patients.https://nmb.abvpress.ru/jour/article/view/600distal arthrogryposis type 5, mechanosensitive ion channel, piezo2 gene
spellingShingle E. L. Dadali
T. V. Markova
E. A. Melnik
S. S. Nikitin
I. V. Sharkova
O. V. Khalanskaya
L. A. Bessonov
E. A. Shestopalova
O. P. Ryzhkova
S. I. Trofimova
O. E. Agranovich
S. I. Kutsev
Expanding the spectrum of clinical and genetic characteristics of distal arthrogryposis type 5 caused by heterozygous variants in the PIEZO2 gene
Нервно-мышечные болезни
distal arthrogryposis type 5, mechanosensitive ion channel, piezo2 gene
title Expanding the spectrum of clinical and genetic characteristics of distal arthrogryposis type 5 caused by heterozygous variants in the PIEZO2 gene
title_full Expanding the spectrum of clinical and genetic characteristics of distal arthrogryposis type 5 caused by heterozygous variants in the PIEZO2 gene
title_fullStr Expanding the spectrum of clinical and genetic characteristics of distal arthrogryposis type 5 caused by heterozygous variants in the PIEZO2 gene
title_full_unstemmed Expanding the spectrum of clinical and genetic characteristics of distal arthrogryposis type 5 caused by heterozygous variants in the PIEZO2 gene
title_short Expanding the spectrum of clinical and genetic characteristics of distal arthrogryposis type 5 caused by heterozygous variants in the PIEZO2 gene
title_sort expanding the spectrum of clinical and genetic characteristics of distal arthrogryposis type 5 caused by heterozygous variants in the piezo2 gene
topic distal arthrogryposis type 5, mechanosensitive ion channel, piezo2 gene
url https://nmb.abvpress.ru/jour/article/view/600
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