MEROSIN-DEFICIENT CONGENITAL MUSCULAR DYSTROPHY (CMD1A): CLINICAL CASE OF CONGENITAL MUSCULAR DYSTROPHY INVOLVING CENTRAL NERVOUS SYSTEM

Congenital muscular dystrophies (CMDs) are an extremely heterogenous group of neuromuscular diseases. The article presents the general information on clinical and pathogenetic aspects of CMD diagnosis with emphasis on one of the most common forms of nervous system disturbances — merosin-deficient co...

Full description

Saved in:
Bibliographic Details
Main Authors: O. A. Klochkova, A. L. Kurenkov, A. M. Mamed'yarov
Format: Article
Language:Russian
Published: Union of pediatricians of Russia 2014-07-01
Series:Педиатрическая фармакология
Subjects:
Online Access:https://www.pedpharma.ru/jour/article/view/77
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849244088549769216
author O. A. Klochkova
A. L. Kurenkov
A. M. Mamed'yarov
author_facet O. A. Klochkova
A. L. Kurenkov
A. M. Mamed'yarov
author_sort O. A. Klochkova
collection DOAJ
description Congenital muscular dystrophies (CMDs) are an extremely heterogenous group of neuromuscular diseases. The article presents the general information on clinical and pathogenetic aspects of CMD diagnosis with emphasis on one of the most common forms of nervous system disturbances — merosin-deficient congenital muscular dystrophy (CMD1A). The authors describe clinical pattern of CMD1A, pathogenesis, epidemiological data, approaches to instrumental, morphological and molecular genetic diagnosis, as well as symptomatic treatment and prenatal diagnosis in detail. As long as there are few genetically confirmed clinical cases of CMD1A described in the publications written in Russian, the authors present their 3-year-long follow-up of a child with genetically confirmed diagnosis of CMD1A (mutations c.2049_2050delAG and c.6993-2A > C of gene LAMA2 [compound heterozygous state]). The article presents a detailed discussion of the described case, comparison with results of recent foreign and Russian observational studies of CMD1A in children. It also contains information on differential diagnosis of CMD1A in the structure of other congenital myodystrophies and optimization of molecular genetic diagnosis.
format Article
id doaj-art-ce57e5c284b7485c8e7cdd9be337d131
institution Kabale University
issn 1727-5776
2500-3089
language Russian
publishDate 2014-07-01
publisher Union of pediatricians of Russia
record_format Article
series Педиатрическая фармакология
spelling doaj-art-ce57e5c284b7485c8e7cdd9be337d1312025-08-20T03:59:16ZrusUnion of pediatricians of RussiaПедиатрическая фармакология1727-57762500-30892014-07-01114818710.15690/pf.v11i4.106977MEROSIN-DEFICIENT CONGENITAL MUSCULAR DYSTROPHY (CMD1A): CLINICAL CASE OF CONGENITAL MUSCULAR DYSTROPHY INVOLVING CENTRAL NERVOUS SYSTEMO. A. Klochkova0A. L. Kurenkov1A. M. Mamed'yarov2Scientific Center of Children’s Health, Moscow, Russian FederationScientific Center of Children’s Health, Moscow, Russian FederationScientific Center of Children’s Health, Moscow, Russian FederationCongenital muscular dystrophies (CMDs) are an extremely heterogenous group of neuromuscular diseases. The article presents the general information on clinical and pathogenetic aspects of CMD diagnosis with emphasis on one of the most common forms of nervous system disturbances — merosin-deficient congenital muscular dystrophy (CMD1A). The authors describe clinical pattern of CMD1A, pathogenesis, epidemiological data, approaches to instrumental, morphological and molecular genetic diagnosis, as well as symptomatic treatment and prenatal diagnosis in detail. As long as there are few genetically confirmed clinical cases of CMD1A described in the publications written in Russian, the authors present their 3-year-long follow-up of a child with genetically confirmed diagnosis of CMD1A (mutations c.2049_2050delAG and c.6993-2A > C of gene LAMA2 [compound heterozygous state]). The article presents a detailed discussion of the described case, comparison with results of recent foreign and Russian observational studies of CMD1A in children. It also contains information on differential diagnosis of CMD1A in the structure of other congenital myodystrophies and optimization of molecular genetic diagnosis.https://www.pedpharma.ru/jour/article/view/77congenital muscular dystrophymerosin-deficient muscular dystrophycmd1amerosinlama2floppy infant syndromemyopathieselectromyographymagnetic resonance imagingmuscle biopsycreatine phosphokinaseneuromuscular diseases
spellingShingle O. A. Klochkova
A. L. Kurenkov
A. M. Mamed'yarov
MEROSIN-DEFICIENT CONGENITAL MUSCULAR DYSTROPHY (CMD1A): CLINICAL CASE OF CONGENITAL MUSCULAR DYSTROPHY INVOLVING CENTRAL NERVOUS SYSTEM
Педиатрическая фармакология
congenital muscular dystrophy
merosin-deficient muscular dystrophy
cmd1a
merosin
lama2
floppy infant syndrome
myopathies
electromyography
magnetic resonance imaging
muscle biopsy
creatine phosphokinase
neuromuscular diseases
title MEROSIN-DEFICIENT CONGENITAL MUSCULAR DYSTROPHY (CMD1A): CLINICAL CASE OF CONGENITAL MUSCULAR DYSTROPHY INVOLVING CENTRAL NERVOUS SYSTEM
title_full MEROSIN-DEFICIENT CONGENITAL MUSCULAR DYSTROPHY (CMD1A): CLINICAL CASE OF CONGENITAL MUSCULAR DYSTROPHY INVOLVING CENTRAL NERVOUS SYSTEM
title_fullStr MEROSIN-DEFICIENT CONGENITAL MUSCULAR DYSTROPHY (CMD1A): CLINICAL CASE OF CONGENITAL MUSCULAR DYSTROPHY INVOLVING CENTRAL NERVOUS SYSTEM
title_full_unstemmed MEROSIN-DEFICIENT CONGENITAL MUSCULAR DYSTROPHY (CMD1A): CLINICAL CASE OF CONGENITAL MUSCULAR DYSTROPHY INVOLVING CENTRAL NERVOUS SYSTEM
title_short MEROSIN-DEFICIENT CONGENITAL MUSCULAR DYSTROPHY (CMD1A): CLINICAL CASE OF CONGENITAL MUSCULAR DYSTROPHY INVOLVING CENTRAL NERVOUS SYSTEM
title_sort merosin deficient congenital muscular dystrophy cmd1a clinical case of congenital muscular dystrophy involving central nervous system
topic congenital muscular dystrophy
merosin-deficient muscular dystrophy
cmd1a
merosin
lama2
floppy infant syndrome
myopathies
electromyography
magnetic resonance imaging
muscle biopsy
creatine phosphokinase
neuromuscular diseases
url https://www.pedpharma.ru/jour/article/view/77
work_keys_str_mv AT oaklochkova merosindeficientcongenitalmusculardystrophycmd1aclinicalcaseofcongenitalmusculardystrophyinvolvingcentralnervoussystem
AT alkurenkov merosindeficientcongenitalmusculardystrophycmd1aclinicalcaseofcongenitalmusculardystrophyinvolvingcentralnervoussystem
AT ammamedyarov merosindeficientcongenitalmusculardystrophycmd1aclinicalcaseofcongenitalmusculardystrophyinvolvingcentralnervoussystem