In 1961 Dreifuss and colleagues described a family with form of muscular dystrophy distinct from more severe Duchenne and ... Becker muscular dystrophies. This syndrome is now designated Emery-Dreifuss muscular dystrophy. With collaborator Kiffin Penry ... Brain 1975;98(3):427-440] [Emery AE, Dreifuss FE (1966). "Unusual type of benign x-linked muscular dystrophy". J. Neurol. ... Dreifuss was born in Dresden, Germany. To escape German state persecution of Jews, the Dreifuss family emigrated to New Zealand ...
Also in the differential are Emery-Dreifuss muscular dystrophies, Pompe disease, later-onset congenital myasthenic syndromes, ... Dystrophinopathies, including Duchenne muscular dystrophy, Becker muscular dystrophy, and manifesting dystrophinopathy in ... Limb-girdle muscular dystrophy (LGMD) is a genetically heterogeneous group of rare muscular dystrophies that share a set of ... which will show the presence of muscular dystrophy, and genetic testing is used to determine which type of muscular dystrophy a ...
... muscular dystrophy, duchenne MeSH C05.651.534.500.350 - muscular dystrophy, emery-dreifuss MeSH C05.651.534.500.400 - muscular ... muscular dystrophy, oculopharyngeal MeSH C05.651.534.500.500 - myotonic dystrophy MeSH C05.651.534.750 - postpoliomyelitis ... muscular dystrophies MeSH C05.651.534.500.074 - distal myopathies MeSH C05.651.534.500.149 - glycogen storage disease type vii ... MeSH C05.651.534.500.280 - muscular dystrophies, limb-girdle MeSH C05.651.534.500.300 - ...
... muscular dystrophy, Duchenne MeSH C16.320.577.350 - muscular dystrophy, Emery-Dreifuss MeSH C16.320.577.400 - muscular ... muscular dystrophy, Duchenne MeSH C16.320.322.625 - muscular dystrophy, Emery-Dreifuss MeSH C16.320.322.750 - oculocerebrorenal ... muscular dystrophy, oculopharyngeal MeSH C16.320.577.500 - myotonic dystrophy MeSH C16.320.700.100 - adenomatous polyposis coli ... corneal dystrophies, hereditary MeSH C16.320.290.162.410 - Fuchs' endothelial dystrophy MeSH C16.320.290.235 - Duane retraction ...
... including Duchenne, Becker, limb girdle, congenital, facioscapulohumeral, myotonic, oculopharyngeal, distal, and Emery-Dreifuss ... Duchenne-Becker muscular dystrophy considerations for adult patients and acute care considerations for all muscular dystrophy ... muscular dystrophies. The act established a Federal Advisory Committee called the Muscular Dystrophy Coordinating Committee ( ... update and disseminate widely existing Duchenne-Becker muscular dystrophy care considerations for pediatric patients, and (2) ...
The cardiac problems that occur with Emery-Dreifuss muscular dystrophy (EDMD) and myotonic muscular dystrophy may require a ... "Duchenne Muscular Dystrophy. What is muscular dystrophy? , Patient". Patient.info. 2016-04-15. Archived from the original on ... Fukuyama congenital muscular dystrophy Muscle hypertrophy Muscular Dystrophy UK Muscular Dystrophy Association (United States) ... Other relatively common muscular dystrophies include Becker muscular dystrophy, facioscapulohumeral muscular dystrophy, and ...
Facioscapulohumeral dystrophy (FSHD) Congenital dystrophy (CMD) Distal (DD) Oculopharyngeal dystrophy (OPMD) Emery-Dreifuss ( ... The most common types include: Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) Myotonic dystrophy Limb- ... There are more than 30 types of muscular dystrophy. Depending on the type, muscular dystrophy can affect the patient's heart ... Multiple diseases can affect the muscular system. Muscular dystrophy is a group of disorders associated with progressive muscle ...
... including Duchenne, Becker, limb girdle, congenital, facioscapulohumeral, myotonic, oculopharyngeal, distal, and Emery-Dreifuss ... Duchenne-Becker muscular dystrophy considerations for adult patients and acute care considerations for all muscular dystrophy ... muscular dystrophies. According to the Muscular Dystrophy Association, "since 2001, there have been 67 clinical trials of drugs ... in carrying out epidemiological activities regarding Duchenne and other forms of muscular dystrophies, to ensure that data from ...
... muscular dystrophy, duchenne MeSH C10.668.491.175.500.350 - muscular dystrophy, emery-dreifuss MeSH C10.668.491.175.500.400 - ... muscular dystrophies MeSH C10.668.491.175.500.074 - distal myopathies MeSH C10.668.491.175.500.149 - muscular dystrophies, limb ... muscular dystrophy, facioscapulohumeral MeSH C10.668.491.175.500.450 - muscular dystrophy, oculopharyngeal MeSH C10.668.491.175 ... muscular atrophy, spinal MeSH C10.228.854.468.800 - spinal muscular atrophies of childhood MeSH C10.228.854.525 - myelitis MeSH ...
Beverly Emanuel Emery-Dreifuss muscular dystrophy - Alan Eglin H. Emery, Fritz E. Dreifuss Erb-Duchenne palsy (a.k.a. Erb palsy ... François-Amilcar Aran Duchenne muscular dystrophy - Guillaume-Benjamin-Amand Duchenne de Boulogne Dukes disease - Clement Dukes ... Eugène Apert Aran-Duchenne disease (a.k.a. Aran-Duchenne spinal muscular atrophy) - François-Amilcar Aran, Guillaume Duchenne ... Pierre-Antoine-Ernest Bazin Becker muscular dystrophy - Peter Emil Becker Beckwith-Wiedemann syndrome - John Bruce Beckwith, ...
... congenital muscular dystrophy (Emery-Dreifuss muscular dystrophy) Collagen VI-related muscular dystrophy (Bethlem myopathy, ... Duchenne muscular dystrophy Becker muscular dystrophy DMD-associated dilated cardiomyopathy Limb girdle muscular dystrophies ( ... Zaspopathy Filaminopathy Bag3opathy Myotonic dystrophy Facioscapulohumeral muscular dystrophy Emery-Dreifuss muscular dystrophy ... Wicklund, MP (December 2019). "The Limb-Girdle Muscular Dystrophies". Continuum (Minneapolis, Minn.). 25 (6): 1599-1618. doi: ...
September 2009). "Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy". American Journal of Human Genetics. 85 ( ... January 2004). "DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy ...
SYNE2 Emery-Dreifuss muscular dystrophy 6; 300696; FHL1 Emery-Dreifuss muscular dystrophy; 310300; EMD Emery-Dreifuss muscular ... ABCC2 Duchenne muscular dystrophy; 310200; DMD Dyggve-Melchior-Clausen disease; 223800; DYM Dysautonomia, familial; 223900; ... LBN Emery-Dreifuss muscular dystrophy 4; 612998; SYNE1 Emery-Dreifuss muscular dystrophy 5; 612999; ... LAMA2 Muscular dystrophy, limb-girdle, type 1A; 159000; TTID Muscular dystrophy, limb-girdle, type 1B; 159001; LMNA Muscular ...
... myopathies Dystrophinopathies Emery-Dreifuss muscular dystrophy In terms of the management of congenital muscular dystrophy the ... which is the second most common type of muscular dystrophy in Japan after Duchenne muscular dystrophy. The founder mutation of ... Muscular dystrophies Ullrich Congenital Muscular Dystrophy Fukuyama Congenital Muscular Dystrophy Sparks, Susan; Quijano-Roy, ... MDC1C also includes Limb-Girdle muscular dystrophy. In terms of the mechanism of congenital muscular dystrophy, one finds that ...
... dominant type Emery-Dreifuss muscular dystrophy, X-linked Emery-Dreifuss muscular dystrophy Emetophobia Emphysema, congenital ... Epstein barr virus mononucleosis Epstein syndrome Equinophobia Erb-Duchenne palsy Erdheim disease Erdheim-Chester disease ... Ellis-Yale-Winter syndrome Ellis-van Creveld syndrome Emerinopathy Emery-Nelson syndrome Emery-Dreifuss muscular dystrophy, ... Epidermodysplasia verruciformis Epidermoid carcinoma Epidermol Epidermolysa bullosa simplex and limb girdle muscular dystrophy ...