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4,352 Possible Causes for MRI Shows Increased Connective Tissue and Fat, Myopathy, Onset of Symptoms in First or Second Decade of Life

  • Limb-Girdle Muscular Dystrophy Type 2L

    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] Keywords Anoctamin-5 Limb-girdle muscular dystrophy Distal myopathy References 1. Bolduc V, Marlow G, Boycott KM, et al.[link.springer.com] […] with early respiratory failure Tibial muscular dystrophy Childhood-onset nemaline myopathy Intermediate nemaline myopathy Severe congenital nemaline myopathy Typical nemaline[csbg.cnb.csic.es]

  • Secondary Myopathy

    Childhood onset weakness, contractures, and early cardiac involvement. Symptoms usually develop in the first or second decade of life.[sites.google.com] We present a family with a distal myopathy secondary to a mutation in myotilin.[eprints.soton.ac.uk] The myopathy is inhibited by prior sciatic nerve section and is accentuated by cholinesterase inhibition.[neurology.org]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • 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] 4, 5 Tropomyosin Hypertrophic cardiomyopathy 3 Nemaline myopathy 1 Titin Hypertrophic cardiomyopathy 9 Other Fibrillin Marfan syndrome Weill–Marchesani syndrome Filamin FG[en.wikipedia.org] , ocular Mitochondrial ocular myopathy Muscular dystrophy Muscular dystrophy, distal Muscular dystrophy, Duchenne Muscular dystrophy, Emery Dreifuss Muscular dystrophy, Erbs[icd9data.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Oculopharyngeal 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] […] some ultrastructural characteristics with distal myopathy with rimmed vacuoles and hereditary inclusion body myopathy.[ncbi.nlm.nih.gov] The question whether oculopharyngodistal myopathy (MIM 164310) is a distinct disease entity or a variant of oculopharyngeal muscular dystrophy (MIM 164300) persists.[ncbi.nlm.nih.gov]

    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] For this reason our finding extends the histological spectrum of myopathies due to ANO5 mutations as well as the possible differential diagnoses for necrotizing myopathy.[ncbi.nlm.nih.gov] In this report, a French family with an autosomal-dominant late-onset distal myopathy of the tibial muscular dystrophy phenotype segregating in several members of the family[ncbi.nlm.nih.gov]

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

    Symptoms Symptom onset usually occurs during the second decade of life, rarely in infancy or adulthood. Facial muscles are affect first.[symptoma.com] OBJECTIVES: To report cases of chronic autoimmune necrotizing myopathy with anti-signal recognition particle antibodies (anti-SRP myopathy) initially misdiagnosed as muscular[ncbi.nlm.nih.gov] Most genetically confirmed FSHD patients exhibit unspecific morphological signs of a degenerative myopathy.[ncbi.nlm.nih.gov]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Kearns-Sayre Syndrome

    Signs and symptoms [ edit ] Individuals with KSS present initially in a similar way to those with typical CPEO. Onset is in the first and second decades of life.[en.wikipedia.org] The syndrome is characterized by chronic progressive external ophthalmoplegia, tapetoretinal degeneration, and severe generalized myopathy.[ncbi.nlm.nih.gov] We present the case of a boy with KSS presenting at the age of 5 years with myopathy, Addison's disease, primary hypoparathyroidism, and Fanconi syndrome.[ncbi.nlm.nih.gov]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Familial Periodic Paralysis

    […] is typically in the first or second decade of life (60% of cases have onset aged 16 years) with susceptible individuals experiencing sudden onset of perioral numbness; weakness[mdedge.com] G72.0 Drug-induced myopathy G72.1 Alcoholic myopathy G72.2 Myopathy due to other toxic agents G72.3 Periodic paralysis G72.4 Inflammatory and immune myopathies, not elsewhere[icd10data.com] NOS G72.8 Other specified myopathies G72.81 Critical illness myopathy Inclusion term(s): Acute necrotizing myopathy Acute quadriplegic myopathy Intensive care (ICU) myopathy[icd10coded.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Hypokalemic Periodic Paralysis

    […] is typically in the first or second decade of life (60% of cases have onset aged 16 years) with susceptible individuals experiencing sudden onset of perioral numbness; weakness[mdedge.com] Other metabolic etiologies of vacuolar myopathy, such as acid phosphatase (lysosomal) associated acid maltase deficiency (a glycogen storage disease), need to be considered[ncbi.nlm.nih.gov] Presenting the case of unusual onset hypokalemic periodic paralysis (HypoPP) where myopathy had developed two years before paralysis occurred.[ncbi.nlm.nih.gov]

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

    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] Bcl-2-associated athanogene-3 (BAG3) mutations have been described in rare cases of rapidly progressive myofibrillar myopathies.[ncbi.nlm.nih.gov] It is described as a neuropathy since the problem originates in the nerves and not in the muscle tissue itself, which would be a myopathy.[uihc.org]

    Missing: MRI Shows Increased Connective Tissue and Fat

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