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3,126 Possible Causes for MRI Shows Increased Connective Tissue and Fat, Muscular Atrophy, Onset of Symptoms in First or Second Decade of Life

  • Limb-Girdle Muscular Dystrophy Type 2L

    . : «Neurogenic muscular atrophy simulating facioscapulohumeral muscular dystrophy». J. Neurol.[jmunozy.org] The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy. Neurology. 2012;78:1714–20. CrossRef PubMed PubMedCentral 10. Flanigan KM.[springermedizin.de]

  • Erb Muscular Dystrophy

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] At that time, the differentiation between the spinal muscular atrophies and weakness associated with central nervous system disorders and primary muscle disease had not been[emedicine.medscape.com] atrophy • proximal weakness • onset of weakness is earlier in childhood • absent deep tendon reflexes and fasciculations • CPK levels are normal • pseudohypertrophy is absent[orthobullets.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Limb-Girdle Muscular Dystrophy

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] atrophy.[ncbi.nlm.nih.gov] […] by Duchenne.1,2 Other descriptions followed: familial atrophy of the pelvic girdle muscles (Leyden in 1876), scapulohumeral muscular atrophy (Erb in 1884), and myopathy with[dash.harvard.edu]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Charcot Marie Tooth Disease

    atrophy Peroneal muscular atrophy Charcot-Marie-Tooth disease、C-M-T[wikidata.org] The onset of clinical symptoms is in the first or second decade of life. Weakness starts distally in the feet and progresses proximally in an ascending pattern.[doi.org] 2015 ICD-9-CM Diagnosis Code 356.1 Peroneal muscular atrophy 2015 Billable Thru Sept 30/2015 Non-Billable On/After Oct 1/2015 ICD-9-CM 356.1 is a billable medical code that[icd9data.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Congenital Muscular Dystrophy

    The objectives of this study were to determine the effects that routine daily home air-stacking maneuvers have on pulmonary function in patients with spinal muscular atrophy[ncbi.nlm.nih.gov] The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] atrophy, forms of Ehlers-Danlos syndrome, and Marfan syndrome (see these terms).[orpha.net]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Young Adult-Onset Distal Hereditary Motor Neuropathy

    Treatment for spinal muscular atrophy Unfortunately, there is currently no specific treatment for SMA.[betterhealth.vic.gov.au] Age of onset is in the second and third decades of life and rarely in the first. Recovery is usually complete and begins weeks to months after the onset of symptoms.[emedicine.medscape.com] […] spinal muscular atrophy Adult onset.[en.wikipedia.org]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Amyotrophic Lateral Sclerosis Type 5

    […] are affected before the distal parts. [6] Thus the pattern of muscular atrophy in our patient differed from that of typical ALS or progressive spinal muscular atrophy in that[neurologyindia.com] It is characterized by onset in the first or second decade of life with slowly progressive weakness and atrophy of the hands and feet and only later bulbar muscles.[academic.oup.com] atrophy and related syndromes G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] G12.1 Other inherited spinal muscular atrophy G12.2 Motor neuron disease G12.21[icd10data.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Myoadenylate Deaminase Deficiency

    The diagnoses in the 13 patients were: polyneuropathy (n 5), infantile spinal muscular atrophy (n 3), congenital myopathy with type 2 fibre atrophy, facioscapulohumeral myopathy[ncbi.nlm.nih.gov] Childhood onset weakness, contractures, and early cardiac involvement. Symptoms usually develop in the first or second decade of life.[sites.google.com] He is currently involved in multiple clinical trials of novel genetic interventions for the treatment of spinal muscular atrophy and Duchenne muscular dystrophy.[books.google.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Friedreich Ataxia

    atrophy, Dr.[sciencedaily.com] Most affected people become wheelchair dependent by the second or third decade of life.[web.archive.org] atrophy and related syndromes G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] G12.1 Other inherited spinal muscular atrophy G12.2 Motor neuron disease Reimbursement[icd10data.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Tay-Sachs Disease

    atrophy.[ncbi.nlm.nih.gov] Late-onset Tay-Sachs disease (chronic form) is a rare variant phenotype with appearance of first symptoms during the second or third decade of life. 4 A juvenile form is also[doi.org] They were first diagnosed as having atypical spinal muscular atrophy and, subsequently, spinocerebellar ataxia, but, recently, the diagnosis of late-onset Tay-Sachs disease[ncbi.nlm.nih.gov]

    Missing: MRI Shows Increased Connective Tissue and Fat

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