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1,746 Possible Causes for Pulverulent Cataract

  • Oculocerebrorenal Syndrome

    Abstract The oculocerebrorenal (Lowe) syndrome is an X-linked recessive disorder characterized by congenital cataracts, hypotonia, developmental delay, poor growth and renal[ncbi.nlm.nih.gov] Oculocerebrorenal syndrome of Lowe (OCRL) is a multisystem disorder characterized by congenital cataracts, hypotonia, and cognitive developmental delay with renal complications[ncbi.nlm.nih.gov] Oculocerebrorenal syndrome (also called Lowe syndrome ) is a rare X-linked recessive disorder characterized by congenital cataracts, hypotonia, intellectual disability, proximal[en.wikipedia.org]

  • 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] Hypomyelination and congenital cataract (HCC) is a rare autosomal recessive white matter disorder characterized by congenital cataract, progressive neurologic impairment,[ncbi.nlm.nih.gov] cataract') characterized by hypomyelination of the central and peripheral nervous system, progressive neurological impairment and congenital cataract.[ncbi.nlm.nih.gov]

  • Maternal Infection

    Congenital cataract following German measles in the mother. 1941. Epidemiol. Infect., 107, iii-xiv; discussion xiii-xiv.[embryology.med.unsw.edu.au]

  • Congenital Cataract

    We found a Chinese family with autosomal dominant pulverulent cataract.[ncbi.nlm.nih.gov] MAF mutations have been reported to cause juvenile-onset pulverulent cataract, microcornea, iris coloboma, and other anterior segment dysgenesis.[ncbi.nlm.nih.gov] Mutations in both Cx46 and Cx50 genes have produced phenotypically similar autosomal dominant lamellar pulverulent cataracts.[doi.org]

  • Cerulean Cataract

    Taylor D: The Doyne Lecture – congenital cataract: the history, the nature and the practice. Eye 1998;12:9–36.[karger.com] Internet Database OMIM: 610202 References OMIM [1] UniProt [2] congenital cerulean cataract 4 (juvenile-onset pulverulent cataracts)[anvita.info] Clinical phenotypes of hereditary congenital cataract are highly heterogeneous.[molvis.org]

  • Lamellar Cataract

    Two Chinese families with pulverulent congenital cataracts and deltaG91 CRYBA1 mutations. Mol Vis. 2007; 13:1154-60.[molvis.org] Another morphologically different autosomal dominant congenital cataract has been linked to the same locus (see Maumenee, 1979).[disorders.eyes.arizona.edu] […] the entire nucleus to pulverulent cataracts involving only the central nucleus or discrete layers Congenital: Zonular (lamellar) Cataract -A circumscribed zone of the lens[quizlet.com]

  • Diabetes in Pregnancy

    Diabetes in pregnancy is still considered a high-risk condition for both mother and baby. Even in the best centres, malformation and mortality rates are reportedly twofold to fivefold higher than in the background population, and pregnancy planning rates remain obstinately poor. Increasing global rates of type 2[…][ncbi.nlm.nih.gov]

  • Autosomal Recessive Congenital Cataract 5

    Congenital cataract is both clinically and genetically heterogeneous; isolated congenital cataract is usually inherited as an autosomal dominant trait although autosomal recessive[bjo.bmj.com] A novel connexin 50 gene (gap junction protein, alpha 8) mutation associated with congenital nuclear and zonular pulverulent cataract.[medsci.org] Keywords Cataract Nonsense Mutation Congenital Cataract Zmax Pakistani Society Background Congenital cataracts show considerable clinical and locus heterogeneity and represent[bmcmedgenet.biomedcentral.com]

  • Coralliform Cataract

    Trans Ophthalmol Soc 30:251–274 Google Scholar He W, Li S (2000) Congenital cataracts: gene mapping.[link.springer.com] , pulverulent, floriform, pisciform, coralliform, or breadcrumb-like cataract.[molvis.org] CTRCT14 includes zonular pulverulent CC cataract, among others.[genome.jp]

  • Fabry Disease

    Fabry disease (MIM 301500) is an X-linked recessive lysosomal storage disorder resulting from deficient α-galactosidase A (α-Gal A) activity. It has been estimated that this disease affects 1 in 50 000 males in the general population. 1,2 α-Gal A is an enzyme involved in the metabolic breakdown of globotriaosylceramide[…][tools.wmflabs.org]

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