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26 Possible Causes for Cataracts Usually Congenital, Conduction Disorder of the Heart

  • Hemochromatosis

    […] levels usually normal or low) II.[faculty.washington.edu] cataracts) Neuroferritinopathy (autosomal dominant genetic disorder affecting basal ganglai; clinical onset in adulthood, iron and ferritin deposits in the brain, ferritin[faculty.washington.edu] H-ferritin mutation Hyperferritinemia without iron overload (autosomal dominant genetic disorder causing high ferritin levels without iron overload; associated with bilateral congenital[faculty.washington.edu]

  • Retinitis Pigmentosa

    Other common symptoms include conduction block (in the heart) and ataxia.[mda.org] In Leber's Disease (26% of R.P. cases), both central and peripheral vision is affected, nystagmus is present, and cataracts do not usually develop; it is congenital.[tsbvi.edu] Types of Mitochondrial Myopathies Kearns-Sayre syndrome (KSS) Onset: Before age 20 Symptoms: This disorder is defined by PEO and pigmentary retinopathy, a “salt-and-pepper[mda.org]

  • Emery-Dreifuss Muscular Dystrophy

    disorders, congestive heart failure, including antiarrhythmic drugs, cardiac pacemaker, implantable cardioverter defibrillator (ICD); heart transplantation for the end stages[checkorphan.org] In some people, the condition can also cause cataracts to develop at a younger age than usual. Life expectancy for people with myotonic dystrophy can vary considerably.[nhs.uk] […] system defects, cardiomyopathy and heart failure.[ncbi.nlm.nih.gov]

  • Emery-Dreifuss Muscular Dystrophy Type 1

    disorders, congestive heart failure, including antiarrhythmic drugs, cardiac pacemaker, implantable cardioverter defibrillator (ICD); heart transplantation for the end stages[checkorphan.org] In some people, the condition can also cause cataracts to develop at a younger age than usual. Life expectancy for people with myotonic dystrophy can vary considerably.[nhs.uk] To the Editor: Lamin A/C gene mutations are associated with various disorders, 1 , 2 including cardiac abnormalities characterized by atrial fibrillation, conduction-system[nejm.org]

  • Muscular Dystrophy-Dystroglycanopathy Type C2

    The progression of the disorder is slow. Heart defects including conduction abnormalities and dilated cardiomyopathy may occur.[rarediseases.org] Walker-Warburg Syndrome Clinical Characteristics Ocular Features: The eyes are usually small and contain either retinal dysplasia or a congenital retinal detachment.[disorders.eyes.arizona.edu] Colobomas, PHPV, cataracts, glaucoma, buphthalmos, anterior chamber dysgenesis, optic atrophy, and optic nerve hypoplasia have also been reported.[disorders.eyes.arizona.edu]

  • Oculopharyngeal Muscular Dystrophy

    Heart conduction gets affected in myotonic dystrophy Heart conduction problems myotonic dystrophy / CFCF / CC A 3.0 The main symptoms of this muscular dystrophy are muscular[muscleatrophy.net] In some people, the condition can also cause cataracts to develop at a younger age than usual. Life expectancy for people with myotonic dystrophy can vary considerably.[nhs.uk] This disorder is also referred to as Myotonia Atrophica Muscular dystrophy. Myotonic Muscular dystrophy is a long term disease which affects many systems of the body.[muscleatrophy.net]

  • Distal Myopathy Type 3

    Heart conduction gets affected in myotonic dystrophy Heart conduction problems myotonic dystrophy / CFCF / CC A 3.0 The main symptoms of this muscular dystrophy are muscular[muscleatrophy.net] In some people, the condition can also cause cataracts to develop at a younger age than usual. Life expectancy for people with myotonic dystrophy can vary considerably.[nhs.uk] This disorder is also referred to as Myotonia Atrophica Muscular dystrophy. Myotonic Muscular dystrophy is a long term disease which affects many systems of the body.[muscleatrophy.net]

  • Optic Atrophy-Intellectual Disability Syndrome

    […] rate) Heart: conduction disorder/arrhythmia (Wolff-Parkinson-White), cardiomyopathy Eyes: optic neuropathy, ophthalmoplegia (eye muscle weakness), retinopathy (abnormal pigmentation[childneurologyfoundation.org] Dislocated lens (usually superiorly and nasally) Severe refractive errors Megalocornea (front third of the eye is larger than normal) Cataracts Uveal colobomas Secondary glaucoma[tsbvi.edu] […] exercise intolerance, myopathy, hypotonia Peripheral nerves: absent reflexes, neuropathic pain, dysautonomia (temperature instability, flushing, fluctuating blood pressure and heart[childneurologyfoundation.org]

  • PHACE Syndrome

    An echocardiogram is a test that uses reflected sound waves to create images of the heart, and can reveal structural heart defects associated with the disorder.[rarediseases.org] […] nerve hypoplasia, congenital cataracts, sclerocornea, lens coloboma, and exophthalmos.[sonoworld.com] An eye doctor will conduct a thorough, extensive eye examination to look for eye abnormalities that may be associated with PHACE syndrome.[rarediseases.org]

  • Myotonic Dystrophy

    Affected individuals will also develop insulin resistance, cataracts, heart conduction defects, testicular atrophy, hypogammaglobulinemia and sleep disorders.[themedicalbiochemistrypage.org] In some people, the condition can also cause cataracts to develop at a younger age than usual. Life expectancy for people with myotonic dystrophy can vary considerably.[nhs.uk] It is characterized by muscle wasting and hypotonia, cataracts, heart conduction defects and endocrinopathies.[icd10data.com]

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