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41 Possible Causes for Cardiomyopathy, Focal Atrophy of Choroid

  • Hemochromatosis

    Lenihan, Infiltrative Cardiomyopathy and Pericardial Disease, Seminars in Oncology, 40, 2, (199), (2013). Hussam Ghoti, Eliezer A.[] The spectral domain optical coherence tomography showed retinal pigmentary epithelial atrophy associated with irregularities and focal interruption of the ellipsoid zone.[] The most common complications of transfusional hemochromatosis are hepatic cirrhosis, hypopituitarism, hypogonadism, diabetes mellitus, other endocrinopathies, and cardiomyopathy[]

  • Mulibrey Nanism Syndrome

    cardiomyopathies; Hereditary Hypertrophic cardiomyopathy Dilated cardiomyopathy Errors of Fatty acid oxidation - 2 disorders of carnitine metabolism (See 1 disorders of Carnitine[] The optic nerve and the macula appeared normal while the midperiphery showed focal choroidal hypoplasia with marked atrophy of the retina and of the pigment epithelium.[] Heart manifestations include constrictive pericarditis and restrictive cardiomyopathy.[]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    1A Dilated cardiomyopathy 1A Dilated cardiomyopathy 1AA Dilated cardiomyopathy 1BB Dilated cardiomyopathy 1C Dilated cardiomyopathy 1D Dilated cardiomyopathy 1E Dilated cardiomyopathy[] Frontometaphyseal dysplasia Gardner syndrome Geroderma osteodysplastica Giant cell glioblastoma Gliosarcoma Glycogen storage disease due to aldolase A deficiency Gyrate atrophy[] -14 Form of dilated cardiomyopathy MYH7 gene Form of scapuloperoneal myopathy Hypertrophic cardiomyopathy-1 Cardiomyopathy, dilated, 1S MYH9 gene Fechtner syndrome May-Hegglin[]

  • Panic Attacks

    ., mitral valve prolapse, hypertension, cardiomyopathy, stroke) are also comorbid factors [22] ; panic patients are nearly twice as likely to develop coronary artery disease[] The ocular findings include: Iridocyclitis Multifocal chorioretinitis Focal areas of chorioretinal atrophy associated with pigmentation Optic neuritis Optic atrophy Sympathetic[] Optic disc nodules/granulomas and/or solitary choroidal nodule. Bilaterality Syphilis Syphilis is a great mimic of panuveitis due to infection with Treponema pallidum.[]

  • High Myopia-Sensorineural Deafness Syndrome

    […] infancy Neuropathy with hearing impairment Oculodentodigital dysplasia Progressive myoclonic epilepsy with dystonia Progressive sensorineural hearing loss - hypertrophic cardiomyopathy[] Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features Sillence syndrome Urogenital adysplasia MOGS-CDG (CDG-IIb) Familial Mediterranean fever Cardiomyopathy[] The cardiomyopathy characteristic of Freidreichs is not seen in Mohr-Tranebjaerg. Norrie Disease.[]

  • Acute Hypertensive Retinopathy

    Nausea & vomiting Confusion Seizures Drowsiness Coma Hypertensive retinopathy Visual disturbance Silver wiring Cotton wool spots Flame haemorrhages Papilloedema Hypertensive cardiomyopathy[] Areas of focal chorioretinal atrophy [from previous choroidal infarcts (Elschnig spots)] are a sign of past episodes of acute HTN.[] A focal area of RPE atrophy was present in the temporal periphery.[]

  • Paraneoplastic Syndrome

    An adult with untreated PDA is at high risk for bacterial endocarditis, an infection of the lining of the heart, valves, or arteries; an enlarged heart (cardiomyopathy); pulmonary[] D) OCT of the same eye demonstrated neurosensory detachment over the macula with focal areas of RPE atrophy and hypertrophy.[] In the adult patient, the prognosis is more dependent on the condition of the pulmonary vasculature and the status of the myocardium if congestive cardiomyopathy was present[]

  • Schwartz-Lelek Syndrome

    ClinGen's adaptation of ACMG's framework to standardize interpretation of MYH7 related cardiomyopathy variants.[] […] of choroid and retina Hereditary spherocytosis Hypomyelination with atrophy of basal ganglia and cerebellum Hypomyelination with brain stem and spinal cord involvement and[] (DCM), Hypertrophic cardiomyopathy (HCM), Myopathy, distal, Myopathy, myosin storage NALCN Congenital contractures of the limbs and face, hypotonia, and developmental delay[]

  • Sorsby Syndrome

    Cardiomyopathy, familial hypertrophic (CAV3) Dilated cardiomyopathy, 1I (DES) Cardiomyopathy, dilated, 3B, X-linked (DMD) Cardiomyopathy, familial hypertrophic, 1 (MYH7)[] The choroid was significantly thinned in areas of atrophy ( L, P ). Figure 4 Clinical findings of family 2.[] Beginning in the midperiphery there are focal areas of choroidal atrophy with well-circumscribed borders separating normal from abnormal tissue.[]

  • Acute Juvenile Hemorrhagic Cystitis

    Mediterranean fever Familial medullary thyroid carcinoma Familial mitral valve prolapse Familial or sporadic hemiplegic migraine Familial paroxysmal ataxia Familial restrictive cardiomyopathy[] […] or choroiditis • Pars plana exudates (“snowbanking”) • Serous, tractional, or rhegmatogenous retinal detachment • Retinochoroidal atrophy • Choroidal and retinal neovascularization[] […] for 4-6 cycles; cumulative dose not to exceed 450-550 mg/m 2 Pediatric Dose Administer as in adults Contraindications Documented hypersensitivity; severe heart failure, cardiomyopathy[]

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