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95 Possible Causes for Isolated Ectopia Lentis, Transillumination of the Iris

  • Ectopia Lentis

    Isolated ectopia lentis usually becomes apparent in childhood. The lens may drift further off-center over time. Vision problems are common in isolated ectopia lentis.[ghr.nlm.nih.gov] Those patients with simple lens ectopia as well as those with ectopic lenses and pupils had striking transillumination of the iris periphery.[ncbi.nlm.nih.gov] The association between ectopia lentis et pupillae and transillumination of the iris is well documented in the literature, but it has never been reported with skin hypopigmentation[ncbi.nlm.nih.gov]

  • Isolated Ectopia Lentis

    Isolated ectopia lentis usually becomes apparent in childhood. The lens may drift further off-center over time. Vision problems are common in isolated ectopia lentis .[ghr.nlm.nih.gov] Transscleral indirect transillumination of the iris did not show any iris pigment epithelial defects.[ijo.in] transillumination, poor pupillary dilatation, persistent pupillary membranes, iridohyaloid adhesions, and prominent iris processes in the anterior chamber angle.[jhu.pure.elsevier.com]

  • Lens Dislocation

    CONCLUSIONS: Late-onset isolated ectopia lentis with secondary glaucoma is consistent with a novel mutation in FBN1.[ncbi.nlm.nih.gov] Ocular Examination  Iris- iridodonesis, transillumination  Appearance of the pupil  assess the adequacy of the pupillary space for a possible aphakic correction  Lens-[slideshare.net] ) ectopia lentis primary ocular disorders aniridia intra-ocular tumors infective conditions, e.g. syphilis Marfan syndrome, homocystinuria and Weill-Marchesania account for[radiopaedia.org]

  • Knobloch Syndrome Type 1

    […] megalocornea Isolated congenital sclerocornea Isolated cryptophthalmia Isolated distichiasis Isolated ectopia lentis Isolated optic nerve hypoplasia/aplasia Juvenile cataract-microcornea-renal[se-atlas.de] Anterior segment abnormalities included absent iris crypts, iris transillumination, lens subluxation, and cataract.[ncbi.nlm.nih.gov] Nettleship-Falls ocular albinism is an X-linked recessive disorder characterized by reduced visual acuity, congenital nystagmus, transillumination defects of the iris ( Fig[clinicalgate.com]

  • Marfan Syndrome

    Mutations in the FBN1 gene have also been observed in families with isolated ectopia lentis and MASS syndrome (myopia, mitral valve prolapse, borderline/non-progressive aortic[genedx.com] Iris transillumination defects (ITD) were significantly more common in MFS eyes (odds ratio for MFS in the presence of ITD, 3.7).[ncbi.nlm.nih.gov] ectopia lentis.[emedicine.com]

  • Glassblower's Cataract

    lentis: isolated and mono-symptomatic. - Marfan's syndrome: characterized by arachnodactyly, long limbs, and laxness of joints. - Weill-Marchesani syndrome: symptoms include[alpfmedical.info] ., Kruckenberg’s spindle), peripheral transillumination of the iris, and increased pigment in the trabcular meshwork may indicate pigmentary dispersion glaucoma.[oogziekenhuis.me] The material appears as white flecks on the pupillary margin of the iris, and it is accompanied by a loss of the pupillary ruff and by peripupillary iris transillumination[glaucomatoday.com]

  • Isolated Congenital Sclerocornea

    Lentis 1, Isolated, Autosomal Dominant Ectopia Lentis, Familial Ectopia Lentis, Isolated Ectopia Lentis, Isolated, Autosomal Dominant ECTOL1 129600 Genetic Test Registry[ukgtn.nhs.uk] transillumination defects, concave iris, increased pigmentation of trabecular meshwork, deposited pigment on Schwalbe’s line/AD/-/%600510 PRADER-WILLI SYNDROME/Refractive[eyewiki.org] lentis and megalocornea Goniodysgenesis Hereditary glaucoma Iridocorneal endothelial syndrome Iridogoniodysgenesis Isolated congenital megalocornea Isolated congenital sclerocornea[se-atlas.de]

  • Autosomal Recessive Isolated Ectopia Lentis 2

    Isolated ectopia lentis usually becomes apparent in childhood. The lens may drift further off-center over time. Vision problems are common in isolated ectopia lentis .[ghr.nlm.nih.gov] There were no areas of iris atrophy, pupillary abnormalities, or iris transillumination in any of the 18 patients examined or their relatives.[cags.org.ae] The iris may transilluminate (67%) and the pupils dilate poorly. Iridodenesis is common (85%). The lens is often malformed and in some cases frankly microspherophakic.[disorders.eyes.arizona.edu]

  • Acrootoocular Syndrome

    Lentis 1, Isolated, Autosomal Dominant Ectopia Lentis, Familial Ectopia Lentis, Isolated Ectopia Lentis, Isolated, Autosomal Dominant ECTOL1 129600 Genetic Test Registry[ukgtn.nhs.uk] transillumination defects, concave iris, increased pigmentation of trabecular meshwork, deposited pigment on Schwalbe’s line/AD/-/%600510 PRADER-WILLI SYNDROME/Refractive[eyewiki.org] transillumination defects, concave iris, increased pigmentation of trabecular meshwork, deposited pigment on Schwalbe's line AD - %600510 PRADER-WILLI SYNDROME Refractive[eyewiki.aao.org]

  • Hereditary Hyperekplexia

    lentis, isolated, autosomal recessive) ADAR (Dyschromatosis symmetrica hereditaria) ADIPOQ (Adiponectin deficiency) ADSL (Adenylosuccinase deficiency) AFF2 (Mental retardation[en.praenatal-medizin.de] transillumination.[amp.pharm.mssm.edu] Thrombotic thrombocytopenic purpura, familial) ADAMTS17 (Weill-Marchesani-like syndrome) ADAMTS2 (Ehlers-Danlos syndrome, type VIIC) ADAMTSL2 (Geleophysic dysplasia) ADAMTSL4 (Ectopia[en.praenatal-medizin.de]

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