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159 Possible Causes for Cataract, Diffuse Hypomyelination

  • Hypomyelinating Leukodystrophy Type 5

    INTERPRETATION: Hypomyelination and congenital cataract is a novel autosomal recessive white matter disorder characterized by the unique association of congenital cataract[ncbi.nlm.nih.gov] Brain magnetic resonance imaging show the combination of a diffuse hypomyelination with superimposed periventricular white matter signal abnormalities. this study describes[ncbi.nlm.nih.gov] In the intermediate stage (approximately 2–10 years), the white matter is diffusely abnormal with a background of diffuse hypomyelination ( Fig 2 ), in most patients associated[ajnr.org]

  • Congenital Cataract

    Note that cataract may affect one or both eyes.[symptoma.com] Brain magnetic resonance imaging show the combination of a diffuse hypomyelination with superimposed periventricular white matter signal abnormalities.[ncbi.nlm.nih.gov] In the intermediate stage (approximately 2–10 years), the white matter is diffusely abnormal with a background of diffuse hypomyelination ( Fig 2 ), in most patients associated[ajnr.org]

  • Cockayne Syndrome

    To describe cataracts in classic and early onset Cockayne syndrome (CS).[ncbi.nlm.nih.gov] Brain imaging reveals diffuse hypomyelination of the cerebral white matter, calcifications in the putamen, and vermian atrophy.[orpha.net] Changes were compatible with diffuse white matter hypomyelination. Basal ganglia calcification was present in both, marked cerebellar atrophy in the older patient.[ncbi.nlm.nih.gov]

  • Congenital Muscular Dystrophy

    Clinical Characteristics Ocular Features: Cataracts have been diagnosed by 6 months of age and may be congenital in origin. Several patients have had strabismus.[disorders.eyes.arizona.edu] Cerebral magnetic resonance imaging revealed diffuse hypomyelination in both cerebral hemispheres; electrophysiological assessment revealed progressive sensorimotor axonal[ncbi.nlm.nih.gov] […] hypoplasia, patchy hypomyelination, and variable callosal hypogenesis and hydrocephalus.[neurologyindia.com]

  • Autosomal Recessive Congenital Cataract 5

    Content covers all details of pediatric cataracts and surgical techniques to treat and prevent visual impairment.[books.google.com] In the intermediate stage (approximately 2–10 years), the white matter is diffusely abnormal with a background of diffuse hypomyelination ( Fig 2 ), in most patients associated[ajnr.org] Treatment Treatment Options: Cataract surgery may be indicated if the opacities are visually significant..[disorders.eyes.arizona.edu]

  • Cataract 35

    Femtosecond laser-assisted cataract surgery versus standard phacoemulsification cataract surgery: Study from the European Registry of Quality Outcomes for Cataract and Refractive[apacrs.org] : Diffuse; Progressive Putamen: Small or Absent Head of the caudate: Reduced size Cerebellar atrophy: Especially granular layer Hypomyelinating Leukodystrophy 9 (HLD9) Arginyl-tRNA[neuromuscular.wustl.edu] الصفحة 58 - TREATMENT OF CATARACT.[books.google.com]

  • Neonatal Adrenoleukodystrophy

    Eye findings include chorioretinopathy, optic nerve dysplasia and cataracts.[orpha.net] (CACH) Childhood Ataxia with Diffuse CNS Hypomyelination (CACH or Vanishing White Matter Disease) Craniometaphysical Dysplasia with Leukoencephalopathy Cystic Leukoencephalopathy[huntershope.org] Eye findings include chorioretinopathy, optic nerve dysplasia and cataracts .[rarediseases.info.nih.gov]

  • Oculo-Palato-Cerebral Syndrome

    Cataract was not mentioned.[dokumen.tips] Sasaki M, Takanashi J, Tada H, et al: Diffuse cerebral hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum. Brain Dev 2009; 31: 582-587.[plaza.umin.ac.jp] Persistent hyperplastic primary vitreous (uni- or bilateral) was present in all cases reported so far and may be associated with microphthalmia, cataract or optic atrophy.[orpha.net]

  • Amaurosis-Hypertrichosis Syndrome

    Rare diseases terms are either (1) terms congenital dominant non nuclear; cataract congenital volkmann type; cataract dental syndrome; cataract hutterite type; cataract hypertrichosis[gilota.xpg.uol.com.br] diffuses central nervous system Macular ataxia myoclonies dégénerescence Ataxia myosis congenital Ataxia opsoclonie myoclonie Ataxia pancytopénie Family paroxystic ataxia[wikipedia.qwika.com] Syndrome Cataract-Dental Syndrome Cataract-Hypertrichosis-Mental Retardation (Cahmr) Syndrome Cataract-Mental Retardation-Hypogonadism Syndrome Cataract-Motor System Disorder-Short[neo-genetics.com]

  • Spastic Ataxia with Congenital Miosis

    […] children, the cataracts are bilateral.[nature.com] MRI shows hypomyelination, as evident from the diffusely elevated T2 white-matter signal.[clinicalgate.com] […] syndrome , Head trauma , Hepatic coma , Human t-lymphotropic virus type i (htlv-i) associated myelopathy , Hydrocephalus , Hyperexplexia , Hypomyelination and congenital cataract[wikidoc.org]

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