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922 Possible Causes for Cardiomyopathy Is Not a Feature

  • Tibial Muscular Dystrophy

    Involvement of the heart consists of usually terminal cardiomyopathy.[] , this is not a consistent feature of any of the major forms of distal myopathy.[] Approximately 20-50% of idiopathic dilated cardiomyopathy (those cases not due to acquired causes) are thought to have a genetic cause.[]

  • Vitamin D Deficiency

    - Symptoms of hypocalcaemia - tetany, stridor, seizure Radiological features - Splaying, fraying and cupping of metaphyses - Osteopenia Principles of treatment Treatment[] […] anterior fontanelle - Frontal bossing - Minimal trauma fractures Non-Bony Signs - Delayed gross motor development - Poor linear growth - Raised intracranial pressure - Dilated cardiomyopathy[]

  • Vitamin B12 Deficiency

    Severe deficiency shows evidence of bone marrow suppression, clear evidence of neurological features, and risk of cardiomyopathy.[] Rarely, cardiomyopathy can occur. 3 Neurological features Neurological impairment includes motor disturbances, sensory loss, abnormal balance and reflexes, cognitive impairment[] However, it is important to recognise that clinical features of deficiency can manifest without anaemia and also without low serum vitamin B12 levels.[]

  • Cardiomyopathy

    Our work extends the phenotypic spectrum of the ALPK3-associated cardiomyopathy by reporting additional clinical features.[] The least common form of cardiomyopathy, restrictive cardiomyopathy, shares many features with hypertrophic cardiomyopathy . Its cause is usually unknown.[] The patient presented dysmorphic features and skeletal deformities of hands and feet, pectus excavatum, and cleft palate.[]

  • Hypertrophic Cardiomyopathy

    BACKGROUND: Interstitial fibrosis, myocardial fiber disarray and non-uniform shortening are common histological features of hypertrophic cardiomyopathy (HCM).[] Macrosomia and hypertrophic cardiomyopathy are two features often associated in neonates of diabetic mothers.[] We report a 10-year-old girl presenting with severe neonatal hypertrophic cardiomyopathy (HCM), feeding difficulties, mildly abnormal facial features, and progressive skeletal[]

  • Ileus

    Takotsubo cardiomyopathy (TCM) is a form of stress-induced cardiomyopathy featured by the dilatation of the apex of the left ventricle during systole.[] Clinical features and outcomes of takotsubo (stress) cardiomyopathy. N Engl J Med. 2015;373:929–38. 12.[] Background Takotsubo cardiomyopathy (TCM) is a form of stress-induced cardiomyopathy, featured by the dilatation of the apex of the left ventricle during systole.[]

  • Peripheral Neuropathy

    The presence of uncommon clinical features (peripheral neuropathy, cardiomyopathy) may result in misdirected molecular diagnostics.[] In some families additional clinical features have been reported.[] , (ii) peripheral neuropathy and cardiomyopathy are rare additional symptoms coexisting with WARBM1, (iii) a pleiotropic effect of a single point mutation is sufficient to[]

  • Acute Amphetamine Intoxication

    Conclusions Amphetamine use is common Look for features of amphetamine toxicity including tachycardia, HTN, sweating and agitation Headache, chest pain and hyperthermia are[] Chronic complications Increased risk of septic emboli e.g. endocarditis, lung/brain abscesses Increased risk of stroke Increased risk of cardiovascular disease including cardiomyopathy[]

  • Orthostatic Hypotension

    , vitreous opacities, & CNS amyloidosis Cardinal feature: slowly progressive sensorimotor & autonomic neuropathy Autonomic neuropathy may be 1st clinical symptom.[] Familial transthyretin amyloidosis TTR AD Slowly progressive peripheral sensorimotor neuropathy & autonomic neuropathy as well as non-neuropathic changes of nephropathy, cardiomyopathy[]

  • Heart Failure

    , a nearly consistent feature in the third decade of life.[] Hydroxychloroquine cardiotoxicity presenting as a rapidly evolving biventricular cardiomyopathy: key diagnostic features and literature review.[] The longer survival of patients with Duchenne muscular dystrophy due to advances in clinical care has increased the incidence of Duchenne muscular dystrophy-associated cardiomyopathy[]

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