Literature DB >> 28181274

Hereditary myopathies with early respiratory insufficiency in adults.

Elie Naddaf1, Margherita Milone1.   

Abstract

INTRODUCTION: Hereditary myopathies with early respiratory insufficiency as a predominant feature of the clinical phenotype are uncommon and underestimated in adults.
METHODS: We reviewed the clinical and laboratory data of patients with hereditary myopathies who demonstrated early respiratory insufficiency before the need for ambulatory assistance. Only patients with disease-causing mutations or a specific histopathological diagnosis were included. Patients with cardiomyopathy were excluded.
RESULTS: We identified 22 patients; half had isolated respiratory symptoms at onset. The diagnosis of the myopathy was often delayed, resulting in delayed ventilatory support. The most common myopathies were adult-onset Pompe disease, myofibrillar myopathy, multi-minicore disease, and myotonic dystrophy type 1. Single cases of laminopathy, MELAS (mitochondrial encephalomyopathy with lactic acidosis and strokelike events), centronuclear myopathy, and cytoplasmic body myopathy were identified.
CONCLUSION: We highlighted the most common hereditary myopathies associated with early respiratory insufficiency as the predominant clinical feature, and underscored the importance of a timely diagnosis for patient care. Muscle Nerve 56: 881-886, 2017.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  congenital myopathy; diaphragm weakness; early respiratory insufficiency; hereditary myopathy; neuromuscular respiratory failure

Mesh:

Substances:

Year:  2017        PMID: 28181274     DOI: 10.1002/mus.25602

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  6 in total

1.  Loss of function variants in DNAJB4 cause a myopathy with early respiratory failure.

Authors:  Conrad C Weihl; Ana Töpf; Rocio Bengoechea; Jennifer Duff; Richard Charlton; Solange Kapetanovic Garcia; Cristina Domínguez-González; Abdulaziz Alsaman; Aurelio Hernández-Laín; Luis Varona Franco; Monica Elizabeth Ponce Sanchez; Sarah J Beecroft; Hayley Goullee; Jil Daw; Ankan Bhadra; Heather True; Michio Inoue; Andrew R Findlay; Nigel Laing; Montse Olivé; Gianina Ravenscroft; Volker Straub
Journal:  Acta Neuropathol       Date:  2022-10-20       Impact factor: 15.887

2.  Predictors of prognosis in type 1 myotonic dystrophy (DM1): longitudinal 18-years experience from a single center.

Authors:  Marco Mazzoli; Alessandra Ariatti; Gian Carlo Garuti; Virginia Agnoletto; Maurilio Genovese; Manuela Gozzi; Shaniko Kaleci; Alessandro Marchioni; Marcella Malagoli; Giuliana Galassi
Journal:  Acta Myol       Date:  2020-09-01

3.  Predictors of respiratory decline in myotonic dystrophy type 1 (DM1): a longitudinal cohort study.

Authors:  Marco Mazzoli; Alessandra Ariatti; Giancarlo Garuti; Virginia Agnoletto; Riccardo Fantini; Alessandro Marchioni; Giuliana Galassi
Journal:  Acta Neurol Belg       Date:  2020-07-10       Impact factor: 2.396

4.  Myopathy With SQSTM1 and TIA1 Variants: Clinical and Pathological Features.

Authors:  Zhiyv Niu; Carly Sabine Pontifex; Sarah Berini; Leslie E Hamilton; Elie Naddaf; Eric Wieben; Ross A Aleff; Kristina Martens; Angela Gruber; Andrew G Engel; Gerald Pfeffer; Margherita Milone
Journal:  Front Neurol       Date:  2018-03-19       Impact factor: 4.003

5.  A Japanese Patient with Hereditary Myopathy with Early Respiratory Failure Due to the p.P31732L Mutation of Titin.

Authors:  Yasuteru Sano; Satoko Ota; Mariko Oishi; Masaya Honda; Masatoshi Omoto; Motoharu Kawai; Mariko Okubo; Ichizo Nishino; Takashi Kanda
Journal:  Intern Med       Date:  2021-10-19       Impact factor: 1.282

Review 6.  The interaction between SARS-CoV-2 and ACE2 may have consequences for skeletal muscle viral susceptibility and myopathies.

Authors:  Peter J Ferrandi; Stephen E Alway; Junaith S Mohamed
Journal:  J Appl Physiol (1985)       Date:  2020-07-16
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.