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142 Possible Causes for Cardiomyopathy, Hypersomnia, Progressive Contractures

  • Muscular Dystrophy

    A pilot study was conducted to assess the safety and efficacy of tranilast in muscular dystrophy patients with cardiomyopathy.[] Walking braces for the ankle-foot or the knee-ankle-foot can help support weak muscles and keep the body flexible, slowing progression of contractures. Medications.[] Apathy and hypersomnia are common features of myotonic dystrophy.[]

  • Chronic Alcoholism

    […] without cardiomyopathy (p 0.001, both) and controls (p 0.05, both).[] Acute renal failure secondary to progressively decreasing renal blood flow (hepatorenal syndrome) may develop.[] Light-to-moderate alcohol intake is associated with a decreased incidence of coronary heart disease, while heavy drinking may be a precursor for cardiomyopathy.[]

  • Myotonic Dystrophy

    Moreover, morphological and functional changes indicative of subclinical cardiomyopathy have been demonstrated by means of cardiac magnetic resonance imaging (CMRI) and spectroscopy[] Shortening of muscles or tendons around joints (contractures). Contractures can further limit mobility. Breathing problems.[] In the later stages of the disease, some people experience sleep apnea and hypersomnia. Women with myotonic dystrophy have an increased risk for pregnancy complications.[]

  • Hereditary Proximal Myopathy with Early Respiratory Failure

    None of the HMERF patients had cardiac involvement, although mutations in TTN are known to cause dilated and hypertrophic cardiomyopathy [ 14 ].[] […] weakness, distal contractures and rigid spine Muscular enolase deficiency Muscular glycogenosis Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome Muscular lipidosis[] Annane D, Moore DH, Barnes PR, Miller RG (2006) Psychostimulants for hypersomnia (excessive daytime sleepiness) in myotonic dystrophy.[]

  • Polyglucosan Body Myopathy Type 2

    1A Dilated cardiomyopathy 1A Dilated cardiomyopathy 1AA Dilated cardiomyopathy 1BB Dilated cardiomyopathy 1C Dilated cardiomyopathy 1D Dilated cardiomyopathy 1E Dilated cardiomyopathy[] Emery-Dreifuss Muscular Dystrophy: Emery-Dreifuss muscular dystrophy is characterized by the triad of joint contractures, slowly progressive muscle weakness and wasting, and[] Foundation – Idiopathic Hypersomnia The Jansen’s Foundation – Jansen Type Metaphyseal Chondrodysplasia The LAMFoundation – Lymphangioleiomyomatosis (LAM) The Life Raft Group[]

  • Oculo-Pharyngo-Distal Myopathy

    Hypersomnia 5. Hypogonadism 6. Mental Retardation 7. Cardiac issues What is the genetic pattern observed in Limb Girdle Muscular Dystrophy Types 1 and 2?[] Electrocardiographic screening was normal and the cardiomyopathy was detected only with echocardiography.[] After prolonged rest Fatigue Back pain Tremor (60%) Joint contractures Distal arthrogryposis Normalize with development Course Childhood: Non-progressive; Contractures resolve[]

  • Hypertrichotic Osteochondrodysplasia

    Diseases related with Cardiomyopathy and Short phalanx of finger In the following list you will find some of the most common rare diseases related to Cardiomyopathy and Short[] Intermittent polyarthralgia results in progressive joint contractures.[] 100,000) Number of published cases or families 422 Idiopathic and/or familial pulmonary arterial hypertension 1.0 P * 88 Idiopathic aplastic anemia 0.4 P * 33208 Idiopathic hypersomnia[]

  • Autosomal Dominant Progressive External Ophthalmoplegia Type 6

    An 11-year-old boy with Kearns-Sayre syndrome developed hypersomnia associated with bithalamic lesions and had complete absence of sleep spindles on a nocturnal polysomnogram[] MTTG MHCM T9997C tRNA Gly nd Rep ( 145 ) Maternally Inherited Cardiomyopathy MTTH MICM G12192A tRNA His - Rep ( 76 ) Cardiomyopathy MTTL2 Dilated Cardiomyopathy T12297C tRNA[] Pes cavus Areflexia Gowers sign Rare Symptoms - Less than 30% cases Abnormal cranial nerve morphology Decreased muscle mass Knee flexion contracture Paralysis Respiratory[]

  • Glycogen Storage Disease due to Phosphoglycerate Mutase Deficiency

    GSD IV GSD IV (brancher deficiency) is associated with myopathy, cardiomyopathy, and liver disease.[] (40%): Shoulders; Hips; Knees; Neck Weight loss Smooth muscle: Urinary or Fecal incontinence Hearing loss Course Progressive Disability related to disease duration 14 Disability[] Lange Syndrome Foundation Stickler Involved People Kawasaki Disease Foundation Klippel-Feil Syndrome Alliance Klippel-Feil Syndrome Freedom Hyperacusis Research Limited Hypersomnia[]

  • Glycogen Storage Disease due to Phosphoglycerate Kinase 1 Deficiency

    Lactic acidosis Anemia Failure to thrive Nephritic syndrome ( FSGS type) Delayed puberty Osteoporosis Neutropenia oral ulcers, GI infections (only in type 1b) Hypertrophic cardiomyopathy[] The disease can progress for several years until death results from cardiorespiratory decompensation.[] Lange Syndrome Foundation Stickler Involved People Kawasaki Disease Foundation Klippel-Feil Syndrome Alliance Klippel-Feil Syndrome Freedom Hyperacusis Research Limited Hypersomnia[]

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