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315 Possible Causes for Lamellar Cataract

  • Foveal Hypoplasia - Presenile Cataract Syndrome

    […] presenting as cerebellar ataxia and pyramidal signs, mental retardation, delays in language development, cretinism, and agenesis of reproductive organs Typically congenital lamellar[obgynkey.com] , blue sclera, pigmentary retinal lesions, and optic atrophy Rothmund–Thomson syndrome (poikiloderma congenitale) Skin atrophy with pigmentary changes and telangiectasis Lamellar[obgynkey.com] […] or punctate cataracts, occasionally band keratopathy, keratoconus, and retinal telangiectasis Werner syndrome (cataract–scleroderma–progeria syndrome) Premature aging, skin[obgynkey.com]

  • Uveal Coloboma - Cleft Lip and Palate - Intellectual Disability

    Infantile spasms Lamellar cataract Capsular cataract Posterior subcapsular cataract Subcapsular cataract Nuclear cataract Amblyopia Congenital cataract Visual loss Coma Milia[mendelian.co] Top matches: Medium match CATARACT 9, MULTIPLE TYPES; CTRCT9 Mutations in the CRYAA gene have been found to cause multiple types of cataract, which have been described as[mendelian.co] […] nuclear, zonular central nuclear, laminar, lamellar, anterior polar, posterior polar, cortical, embryonal, anterior subcapsular, fan-shaped, and total.[mendelian.co]

  • Lamellar Cataract

    […] of dominantly inherited lamellar cataract in individuals of different ages in the same family.[ncbi.nlm.nih.gov] We present data on the recreation of the human lamellar cataract phenotype in transgenic mice.[ncbi.nlm.nih.gov] Here, we demonstrate via BAC (bacterial artificial chromosome) transgenesis that p.Arg116His recreates the childhood lamellar cataract in mice suggesting that incomplete penetrance[ncbi.nlm.nih.gov]

  • Traumatic Cataract

    Forms of hereditary congenital cataract: Lamellar or zonular cataract.[alpfmedical.info] […] with high astigmatism after deep anterior lamellar keratoplasty (DALK).[ncbi.nlm.nih.gov] […] the embryonic hyaloid artery on the posterior capsule of the lens; see Chapter 11). — Lamellar cataract.[alpfmedical.info]

  • Cataract

    Cloudiness can occur in one or more parts of the lens: A lamellar cataract is cloudiness between the nuclear and cortical layers of the lens [See figure 3] A nuclear cataract[aapos.org]

  • Neonatal Jaundice

    The second patient, a boy of Maltese extraction who was found to have bilateral lamellar cataracts at the age of 4 years, was identified as G6PD deficient only as a result[ncbi.nlm.nih.gov]

  • Metaphyseal Chondrodysplasia - Retinitis pigmentosa Syndrome

    cataract (one type) Langer–Giedion syndrome Lesch–Nyhan syndrome Li–Fraumeni syndrome Limb–girdle muscular dystrophy 2b Lowe syndrome Lymphoproliferative syndrome Macular[easternbiotech.com] […] nigricans Interleukin 2 deficiency Intestinal aganglionosis (Hirschsprung) Isovalericacidemia Juvenile myoclonic epilepsy Kallmann syndrome 17-Ketosteroid reductase deficiency Lamellar[easternbiotech.com]

  • Retinitis Pigmentosa 32

    , Kyphosis Syndrome Cataract, Nuclear Diffuse Nonprogressive Cataract, Nuclear Progressive Cataract, Polymorphic and Lamellar Cataract, Posterior Polar, 1 Cataract, Posterior[rgd.mcw.edu] , Cortical, Juvenile-Onset Cataract, Crystalline Aculeiform Cataract, Crystalline Coralliform Cataract, Juvenile, with Microcornea and Glucosuria Cataract, Microcephaly, Arthrogryposis[rgd.mcw.edu] , Congenital, with Mental Impairment and Dentate Gyrus Atrophy Cataract, Congenital, with Microcornea or Slight Microphthalmia Cataract, Cortical Pulverulent, Late-Onset Cataract[rgd.mcw.edu]

  • Retinitis pigmentosa, Y-Linked

    cataract (one type) Langer–Giedion syndrome Lesch–Nyhan syndrome Li–Fraumeni syndrome Limb–girdle muscular dystrophy 2b Lowe syndrome Lymphoproliferative syndrome Macular[easternbiotech.com] […] nigricans Interleukin 2 deficiency Intestinal aganglionosis (Hirschsprung) Isovalericacidemia Juvenile myoclonic epilepsy Kallmann syndrome 17-Ketosteroid reductase deficiency Lamellar[easternbiotech.com]

  • Cataract - Congenital Heart Disease - Neural Tube Defect Syndrome

    Posterior subcapsular and lamellar cataracts are non-specific and non-diagnostic.[jmg.bmj.com] Berry V, Francis P, Kaushal S, Moore A, Bhattacharya S: Missense mutations in MIP underlie autosomal dominant ‘polymorphic' and lamellar cataracts linked to 12q.[karger.com] […] opacities, a lamellar component, and an unusual, subcapsular, diffuse, wispy consistency noted at surgery.[jmg.bmj.com]

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