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1,939 Possible Causes for Myotonic Dystrophy, Subcortical White Matter Lesions in the Temporal Lobes (MRI)

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  • Myotonic Dystrophy

    Myotonic dystrophy is of 2 types; namely: myotonic dystrophy type 1 and myotonic dystrophy type 2.[symptoma.com] Peter Harper, "Myotonic Dystrophy: The Facts"[web.archive.org] A variation of type 1 myotonic dystrophy, called congenital myotonic dystrophy, is apparent at birth.[web.archive.org]

  • Pilomatrixoma

    Multiple and familial cases of pilomatrixomas have been reported in myotonic dystrophy. We report 2 cases of pilomatrixoma in Turner's syndrome.[ncbi.nlm.nih.gov] There is evidence to suggest that patients with a family history of multiple pilomatrixomas have a high probability of autosomal dominant disorders such as myotonic dystrophy[ncbi.nlm.nih.gov] Links: myotonic dystrophy[gpnotebook.co.uk]

    Missing: Subcortical White Matter Lesions in the Temporal Lobes (MRI)
  • Muscular Dystrophy

    However, defects in CLCN1 disrupt ion flow, Read More In muscle disease: Myotonic diseases Myotonic dystrophy is the most common of the myotonic disorders.[britannica.com] RNA pathogenesis of the myotonic dystrophies.[ncbi.nlm.nih.gov] Cardiac involvement in Steinert's myotonic dystrophy.[web.archive.org]

    Missing: Subcortical White Matter Lesions in the Temporal Lobes (MRI)
  • Ptosis

    Bilateral ptosis in the setting of myotonic dystrophy.[eyerounds.org] ,myotonic dystrophy, chronic progressive external opthalmoplegia.[iovs.arvojournals.org] Myotonic dystrophy Myotonic dystrophy is a hereditary condition with autosomal dominant inheritance. It is the most common form of adult-onset muscular dystrophy.[eyerounds.org]

    Missing: Subcortical White Matter Lesions in the Temporal Lobes (MRI)
  • Arthrogryposis due to Muscular Dystrophy

    dystrophy, congenital muscular dystrophy myotubular myopathy, and craniocarpotarsal dysplasia.[miami.pure.elsevier.com] Z Orthop Chir 14:52–67 Google Scholar Sarnat HS, Silbert SW (1976) Maturational arrest of fetal muscle in neonatal myotonic dystrophy.[link.springer.com] […] muscular atrophy, Moebious syndrome, congenital hypomyelinating neuropathy, transient congenital myasthenia gravis, infant of mother with multiple sclerosis, congenital myotonic[miami.pure.elsevier.com]

    Missing: Subcortical White Matter Lesions in the Temporal Lobes (MRI)
  • CADASIL Syndrome

    ) diffuse periventricular and deep white matter lesions subcortical infarcts in white matter, basal ganglia, and brain stem external capsules and temporal lobes are often[en.wikibooks.org] dystrophy type 1 think of it in younger patients with small vessel ischemic white matter change predilection for anterior temporal lobe white matter is a distinctive feature[radiopaedia.org] Myotonic Dystrophy Type 1 Thomas D Bird. Initial Posting: September 17, 1999; Last Revision: December 6, 2018.[ncbi.nlm.nih.gov]

  • Secondary Myopathy

    Myotonic dystrophy [Internet]. Yale school of Medicine. [updated 2013 February 14]. Available from: 8.[chanrejournals.com] dystrophy DM1, Proximal myotonic myopathy (Myotonic dystrophy DM2), Myotonia Congenita (Thomsen’s disease) Dermatomyositis , polymyositis Drug toxicity Denervation: Motor[learningneurology.com] Muscular Dystrophy. The two main dystrophies with ophthalmoplegia are myotonic dystrophy and oculopharyngeal dystrophy.[neuroophthalmology.ca]

    Missing: Subcortical White Matter Lesions in the Temporal Lobes (MRI)
  • Emery-Dreifuss Muscular Dystrophy Type 1

    Practical suggestions for the anesthetic management of a myotonic dystrophy patient. Myotonic dystrophy foundation toolkit. 2013;73-80. [Cited 2017 Feb 6].[scielo.org.co] Myotonic dystrophy As with other types of muscular dystrophy, myotonic dystrophy involves progressive muscle weakness and muscle wasting.[nhs.uk] Assessment of a diseasespecific muscular impairment raiting scale in myotonic dystrophy. Neurology 2001;56:336-340. [ Links ][scielo.org.co]

    Missing: Subcortical White Matter Lesions in the Temporal Lobes (MRI)
  • Oculo-Pharyngo-Distal Myopathy

    dystrophy type 1 (DM1), which is caused by an unstable, expansile CTG trinucleotide repeat in the gene myotonic dystrophy type 1 protein kinase (DMPK) on chromosome 19 Demonstrates[evidencereviewed.com] , myotonic dystrophy type 1 and multi-minicore disease associated to RYR1 mutations.[ncbi.nlm.nih.gov] Myotonic dystrophy Congenital myopathy Hyperparathyroidism 17.[de.slideshare.net]

    Missing: Subcortical White Matter Lesions in the Temporal Lobes (MRI)
  • Limb-Girdle Muscular Dystrophy Type 1E

    […] in adults especially with European ancestry risk factors family history Etiology genetics myotonic dystrophy (MD) type 1 autosomal dominant mutation in DMPK gene on chromosome[medbullets.com] MYOTONIC DYSTROPHY Myotonic dystrophy Myotonic dystrophy. Three ring fibers (one marked), atrophic myofibers, and central nuclei.[neuropathology-web.org] Duchenne muscular dystrophy is the most common form affecting children. Myotonic dystrophy type 1 is the most common form affecting adults.[my.clevelandclinic.org]

    Missing: Subcortical White Matter Lesions in the Temporal Lobes (MRI)

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