نتایج جستجو برای: facioscapulohumeralmuscular dystrophy

تعداد نتایج: 22674  

Journal: :British medical journal 1967
A E Emery E R Clack S Simon J L Taylor

From the point of view of genetic counselling carrier detection is most important in X-linked disorders. Okinaka et al. (1959) were the first to employ the serum level of creatine kinase to detect female carriers of X-linked Duchenne muscular dystrophy. Since then many investigators have confirmed the usefulness and reliability of this test. So far results on over 200 carriers have been reporte...

Journal: :Neuromuscular disorders : NMD 2003
K Bushby F Muntoni J P Bourke

Sixteen participants from Austria, France, Germany, Italy, the Netherlands and the UK met to discuss the cardiac implications of the diagnosis of muscular dystrophy and myotonic dystrophy. The group included both myologists and cardiologists from nine different European centers. The aims of the workshop were to agree and report minimum recommendations for the investigation and treatment of card...

Journal: :Brain : a journal of neurology 2011
Karen Anthony Sebahattin Cirak Silvia Torelli Giorgio Tasca Lucy Feng Virginia Arechavala-Gomeza Annarita Armaroli Michela Guglieri Chiara S Straathof Jan J Verschuuren Annemieke Aartsma-Rus Paula Helderman-van den Enden Katherine Bushby Volker Straub Caroline Sewry Alessandra Ferlini Enzo Ricci Jennifer E Morgan Francesco Muntoni

Duchenne muscular dystrophy is caused by mutations in the DMD gene that disrupt the open reading frame and prevent the full translation of its protein product, dystrophin. Restoration of the open reading frame and dystrophin production can be achieved by exon skipping using antisense oligonucleotides targeted to splicing elements. This approach aims to transform the Duchenne muscular dystrophy ...

2014
G. Remmers D. W. Hayden M. A. Jaeger J. M. Ervasti S. J. Valberg

There are few reports of naturally occurring muscular dystrophy in domestic animals. Herein, we describe a case of muscular dystrophy in a 4-year-old neutered male American domestic shorthair cat that died unexpectedly following anesthesia for an elective surgical procedure. Macroscopic muscular hypertrophy and histologic evidence of myofiber size variation, mineralization, myofiber degeneratio...

2002
GEOFFREY MILLER ALAN H. BEGGS Milton S. Hershey

-We present two cases of autosomal dominant limb girdle muscular dystrophy in a father and son. Both presented in childhood with a classical Becker muscular dystrophy phenotype. The father had initially been informed that he would not have affected children. After the diagnosis of muscular dystrophy in the son, immunoblot analysis was performed on muscle and revealed normal dystrophin. The poly...

Journal: :Anesthesiology 2021

I read with great interest the short report published in Images Anesthesiology section about difficult intubation a 2-yr-old patient Ullrich congenital muscular dystrophy.1 This disease is well known to carry risk of intubation.2–6 The authors nicely described how they used nasopharyngeal airway administer volatile anesthetic and oxygen through one nostril while performing nasotracheal fiberopt...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2001
C Ertekin N Yüceyar Aydoğdu H Karasoy

OBJECTIVE Oropharyngeal dysphagia is a common feature of patients with myotonic dystrophy and is not usually perceived due to their emotional deficits and lack of interest. The aim was to show the existence and frequency of subclinical electrophysiological abnormalities in oropharyngeal swallowing and to clarify the mechanisms of dysphagia in myotonic dystrophy. METHODS Eighteen patients with...

Journal: :The Ulster Medical Journal 1994
M. Avaria V. Patterson

Twenty-five symptoms, signs, and abnormal investigations were looked for in 20 patients with clinically-definite myotonic dystrophy. Weakness of facial muscles, neck flexors, and arm external rotators was found in all patients (sensitivity = 100%). Arm external rotation has not been reported as a frequently involved muscle in previous clinical studies on myotonic dystrophy. Careful examination ...

2016
Sabrina Giacoppo Thangavelu Soundara Rajan Rocco Salvatore Calabrò Placido Bramanti Emanuela Mazzon

Facioscapulohumeral dystrophy (FSHD) is the third most common type of muscular dystrophy after Duchenne and myotonic dystrophy with an incidence of 12 per 100,000 worldwide [1,2]. FSHD is an autosomal dominant disease with an insidious onset and development, characterized by progressive weakness and atrophy of facial, shoulder girdle and upper arm muscles [1]. Currently FSHD diagnosis is mainly...

Journal: :Arthritis care & research 2013
Gulnara Mamyrova James D Katz Robert V Jones Ira N Targoff Peter A Lachenbruch Olcay Y Jones Frederick W Miller Lisa G Rider

OBJECTIVE To differentiate juvenile polymyositis (PM) and muscular dystrophy, both of which may present with chronic muscle weakness and inflammation. METHODS We studied 39 patients with probable or definite juvenile PM and 9 patients with muscular dystrophies who were initially misdiagnosed as having juvenile PM. Differences in demographic, clinical, and laboratory results; outcomes; and tre...

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