The cardiac problems that occur with Emery–Dreifuss muscular dystrophy (EDMD) and myotonic muscular dystrophy may require a pacemaker. The myotonia (delayed...
30 KB (2,269 words) - 03:51, 8 November 2024
Emery–Dreifuss muscular dystrophy (EDMD) is a type of muscular dystrophy, a group of heritable diseases that cause progressive impairment of muscles. EDMD...
21 KB (1,627 words) - 01:14, 24 October 2024
Facioscapulohumeral muscular dystrophy can appear similarly, especially when it spares the facial muscles. Also in the differential are Emery–Dreifuss muscular dystrophies...
35 KB (2,822 words) - 01:57, 6 November 2024
Facioscapulohumeral dystrophy (FSHD) Congenital dystrophy (CMD) Distal (DD) Oculopharyngeal dystrophy (OPMD) Emery-Dreifuss (EDMD) Major systems of the human body...
15 KB (1,733 words) - 23:05, 12 November 2024
congenital muscular dystrophy (Emery–Dreifuss muscular dystrophy) Collagen VI-related muscular dystrophy (Bethlem myopathy, Ullrich congenital muscular dystrophy)...
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myosclerosis Bethlem myopathy Ehlers–Danlos syndrome Emery–Dreifuss muscular dystrophy Limb-girdle muscular dystrophy RYR1-associated multiminicore disease Phenotypes...
15 KB (1,320 words) - 14:36, 24 August 2024
myopathies Dystrophinopathies Emery-Dreifuss muscular dystrophy In terms of the management of congenital muscular dystrophy the American Academy of Neurology...
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Emerin (redirect from EMD (muscular dystrophy))
X-linked recessive Emery–Dreifuss muscular dystrophy, cardiac conduction abnormalities and dilated cardiomyopathy. It is named after Alan Emery. Emerin is a...
20 KB (2,339 words) - 06:42, 2 November 2024
Bethlem myopathy 1 or 2, which helps to differentiate it from Emery–Dreifuss muscular dystrophy. Currently there is no cure for the disease and symptomatic...
23 KB (2,333 words) - 19:52, 23 August 2024
Emery–Nelson syndrome Emery–Dreifuss muscular dystrophy, dominant type Emery–Dreifuss muscular dystrophy, X-linked Emery–Dreifuss muscular dystrophy Emetophobia...
12 KB (918 words) - 00:54, 17 August 2024
Gisèle (2 September 2015). "Laminin α2 Deficiency-Related Muscular Dystrophy Mimicking Emery-Dreifuss and Collagen VI related Diseases". Journal of Neuromuscular...
36 KB (3,710 words) - 08:53, 9 November 2024
Jill Viles (category People with muscular dystrophy)
is an American writer recognized for her self-discovery of Emery-Dreifuss muscular dystrophy. Jill Viles was born in Des Moines, Idaho, in 1974, the eldest...
12 KB (1,217 words) - 16:40, 10 September 2024
Laminopathy (category Muscular dystrophy)
envelopathy with the highest frequency in human populations is Emery–Dreifuss muscular dystrophy caused by an X-linked mutation in the EMD gene coding for...
33 KB (3,435 words) - 07:57, 5 November 2024
remains. For instance, some individuals with Duchenne and Becker muscular dystrophy may start with true muscle hypertrophy, but later develop into pseudohypertrophy...
85 KB (5,216 words) - 07:42, 11 November 2024
Becker's muscular dystrophy Mitochondrial myopathy Polyneuropathy and metabolic myopathy Genetic related Emery–Dreifuss muscular dystrophy Myotubular...
23 KB (2,386 words) - 20:46, 11 October 2024
several diseases, including Emery–Dreifuss muscular dystrophy, familial partial lipodystrophy, limb girdle muscular dystrophy, dilated cardiomyopathy, Charcot–Marie–Tooth...
24 KB (2,694 words) - 22:56, 9 April 2024
congenital muscular dystrophy (CMD) (L-CMD, congenital muscular dystrophy associated to the LMNA gene or Emery-Dreifuss muscular dystrophy II) is a disease...
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Both Emery–Dreifuss muscular dystrophy and its defective protein product, emerin, are named after him (the former jointly with Fritz E. Dreifuss)). Peter...
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implicated in a variety of diseases (laminopathies) such as: Emery–Dreifuss muscular dystrophy - A muscle wasting disease Progeria - Premature aging Restrictive...
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recombination, son of R. A. Emerson Alan Emery (born 1928), British neuromuscular geneticist, Emery–Dreifuss muscular dystrophy Boris Ephrussi (1901–1979), Russian-born...
71 KB (7,873 words) - 14:30, 19 November 2024
The Jerry Lewis MDA Labor Day Telethon (redirect from Muscular dystrophy telethon)
in the United States to raise money for the Muscular Dystrophy Association (MDA). The Muscular Dystrophy Association was founded in 1950 with hopes of...
114 KB (12,651 words) - 11:20, 17 November 2024
Paul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education Amendments of 2013
muscular dystrophy, including Duchenne, Becker, limb girdle, congenital, facioscapulohumeral, myotonic, oculopharyngeal, distal, and Emery–Dreifuss muscular...
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an Iowa mother without any medical training but who had Emery–Dreifuss muscular dystrophy and who spotted physical similarities between herself and...
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of X-linked Emery–Dreifuss muscular dystrophy. As mutations in lamins cause the autosomal dominant form of Emery–Dreifuss muscular dystrophy, and lamins...
14 KB (1,711 words) - 03:06, 26 August 2024
et al. (September 2009). "Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy". American Journal of Human Genetics. 85 (3): 338–353. doi:10...
50 KB (4,445 words) - 04:08, 16 June 2024
Emanuel syndrome – Beverly Emanuel Emery–Dreifuss muscular dystrophy – Alan Eglin Heathecote Emery, Fritz E. Dreifuss Erb–Duchenne palsy (a.k.a. Erb palsy)...
63 KB (6,565 words) - 18:27, 15 November 2024
University (2007–2011) Jill Viles, writer known for having Emery-Dreifuss muscular dystrophy and Partial lipodystrophy Oshoke Pamela Abalu (born 1978)...
62 KB (6,256 words) - 07:51, 17 November 2024
pension financed by the government.) Fritz E. Dreifuss, American physician – Emery–Dreifuss muscular dystrophy Dubgall mac Somairle, King of the Isles – Clann...
117 KB (11,145 words) - 15:55, 10 November 2024
muscular dystrophy, including Duchenne, Becker, limb girdle, congenital, facioscapulohumeral, myotonic, oculopharyngeal, distal, and Emery–Dreifuss muscular...
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"Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy". Human Molecular Genetics. 6 (13): 2257–2264. doi:10.1093/hmg/6...
107 KB (12,347 words) - 05:01, 2 November 2024