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19 Possible Causes for Cardiomyopathy, Onset between 6 and 14 Years

  • Limb-Girdle Muscular Dystrophy

    This is the first report showing the electron microscopic findings of dilated cardiomyopathy (DCM) accompanied with limb girdle muscular dystrophy.[ncbi.nlm.nih.gov] Early motor milestones: Most normal; Toe walking common Range: 2 to 45 years; Median 14 to 20 years; 71% between 6 to 18 years Weakness: Proximal legs; Rectus abdominus No[neuromuscular.wustl.edu] This may manifest as hypertrophic/dilated cardiomyopathy and cardiac dysrhythmias.[circheartfailure.ahajournals.org]

  • Progressive Myoclonic Epilepsy Type 7

    .  Affected individuals sometimes have short stature and heart abnormalities, cardiomyopathy.  Mutations in the MT-TK gene are the most common cause of MERRF, occurring[slideshare.net] RETARDATION, X-LINKED TYPE 90 Shank3 (N69/46) CHROMOSOME 22q13.3 DELETION SYNDROME Slo1 (L6/60) GENERALIZED EPILEPSY AND PAROXYSMAL DYSKINESIA Tafazzin (N173B/13) BARTH SYNDROME CARDIOMYOPATHY[neuromab.ucdavis.edu] A novel combination of mitochondrial tRNA and ND1 gene mutations in a syndrome with MELAS, cardiomyopathy, and diabetes mellitus. Hum Mutat. 1996;7(4):358-60.[stoffwechselerkrankungen.de]

  • Distal Myopathy Type 3

    Involvement of the heart consists of usually terminal cardiomyopathy.[icd9data.com] Age of onset of initial symptoms varied between patients: In family A (Fig. 1A ), while patient 6 was symptomatic already at 2 years of age, patients 1, 5 and 7 recall initial[bmcmedgenet.biomedcentral.com] The cardiomyopathy phenotype is usually classified as dilated cardiomyopathy (DCM) but also ARVC and hypertrophic cardiomyopathies (HCM) have been described.[blueprintgenetics.com]

  • Panayiotopoulos Syndrome

    […] age 20 years Clinical features: Early – progressive myoclonic epilepsy, GTC seizures, ataxia, action-induced polymyoclonus Late – progressive muscle weakness, hypertrophic cardiomyopathy[emilytam.com] Clinical context Panayiotopoulos syndrome is characterized by onset of seizures between 1 and 14 years of age (majority between 3 and 6 years).[epilepsydiagnosis.org] Panayiotopoulos syndrome is characterized by onset of seizures between 1 and 14 years of age (majority between 3 and 6 years).[medlink.com]

  • Acute Disseminated Encephalomyelitis

    We present here a case of atypical Takotsubo cardiomyopathy arising as a result of a lesion in the medulla oblongata.[ncbi.nlm.nih.gov] In this study, all 15 patients who fell ill within 2 months before the onset (6 cases: 14 years old; 5 cases: 15–59 years old; 4 cases: 60 years old) had a history of preceding[bmcpublichealth.biomedcentral.com] Cardiomyopathy is a particularly concerning effect as it is irreversible; thus regular monitoring with echocardiograms or MUGA scans is recommended for patients.[en.wikipedia.org]

  • Behçet Disease

    Cardiac involvement is very rare but can occur with different presentations including: pericarditis, cardiomyopathy, endocarditis, endomyocardial fibrosis, intracavitary thrombosis[dx.doi.org] […] as long as 14 years. 5 Conversely, intraocular inflammation is the presenting feature in over 10% of patients, 6 and in rare cases oral aphthosis may not occur at all. 7 The[doi.org] Hamid Khederlou, Samin Taheri, Alireza Sadeghi and Amirhossein Moghtader Mojdehi, Dilated Cardiomyopathy in Behcet′s Disease in a Young Male Patient, International Journal[dx.doi.org]

  • Congenital Cytomegalovirus Infection

    Fetal echocardiography performed during pregnancy showed impaired LV function, suggesting that the cardiomyopathy was associated with cytomegalovirus infection in utero.[ncbi.nlm.nih.gov] The subjects included 19 healthy adults (9 men and 10 women between 21 and 29 years old), 7 patients with adult‐onset Still disease, and 14 patients with other connective[doi.org] […] tissue diseases (such as systemic lupus erythematosus [ 6 ], rheumatoid arthritis [ 3 ], systemic sclerosis [ 2 ], poliomyelitis [ 1 ], and mixed connective tissue disease[doi.org]

  • Diffuse Cerebral Sclerosis of Schilder

    […] hypertrophic subaortic stenosis, obstructive hypertrophic cardiomyopathy Ontology Lookup Service immune system disease autoimmune disease nec, autoimmune disease, not elsewhere[hpscreg.eu] Epidemiology and Demographics The disorder usually begins in childhood with an age of onset between 5 and 14 years old. [4] [5] Natrual History, Complication and Prognosis[wikidoc.org] […] spondyloarthritis, ankylosing Ontology Lookup Service anti-social behavior Ontology Lookup Service Aplastic anemia Ontology Lookup Service Arrhythmogenic right ventricular cardiomyopathy[hpscreg.eu]

  • Amaurotic Familial Idiocy

    During Pregnancy Alcohol problems: Helping someone get treatment Alcohol problems: How to stop drinking Alcohol, Fetal Effects of Alcohol-Related Birth Defects Alcoholic Cardiomyopathy[healthmedicinet.com] Amaurotic Idiocy (onset after 1 year) - Bielschowski's form; Juvenile Amaurotic Idiocy (between ages of 6 and 14 years) - Spielmeyer-Vogt's form; Late Amaurotic Idiocy (onset[scielo.br] Complementary and alternative medicine - Patient Information [NCI] ARPKD Arrhythmias and Sexual Activity Arrhythmias: Foods That Affect Heart Rate Arrhythmogenic Right Ventricular Cardiomyopathy[healthmedicinet.com]

  • Intermittent Hydrarthrosis

    […] fatty liver of pregnancy Autosomal recessive nonsyndromic intellectual deficit Autosomal recessive nonsyndromic sensorineural deafness type DFNB Baraitser-Winter syndrome Cardiomyopathy[csbg.cnb.csic.es] [12] Case reports indicate that only white people are affected. [3] [14] First onset of IH is most common between the ages of 20 and 50 years, and in females, onset can often[en.wikipedia.org] […] deficiency Mitochondrial trifunctional protein deficiency Polymicrogyria due to TUBB2B mutation Primary dystonia, DYT4 type Progressive sensorineural hearing loss - hypertrophic cardiomyopathy[csbg.cnb.csic.es]

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