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1,049 Possible Causes for Ectopia Lentis, Myopia

  • Marfan Syndrome

    We present a case of Marfan syndrome with lens coloboma in one eye and ectopia lentis in the other. A 14-year-old girl reported decreased vision in the left eye.[ncbi.nlm.nih.gov] The emergence of additional clinical signs (marfanoid habitus, severe myopia and dilatation of the aortic bulb) lead to consider the diagnosis of the progeroid variant of[ncbi.nlm.nih.gov] A related disorder, dominant ectopia lentis (EL), has also been linked genetically to this locus.[doi.org]

  • Homocystinuria

    KEYWORDS: Ectopia lentis; Homocystinuria; Non-traumatic; Pakistan[ncbi.nlm.nih.gov] Further investigations disclosed lens subluxation in association with myopia, mild scoliosis and osteopenia.[ncbi.nlm.nih.gov] Homocystinuria due to cystathionine-β-synthase deficiency (CBS deficiency) usually presents with ectopia lentis, myopia, intellectual disability, skeletal anomalies resembling[ncbi.nlm.nih.gov]

  • Ectopia Lentis

    Ectopia lentis. Dislocated lens into the vitreous secondary to trauma. Ectopia lentis.[emedicine.com] Identification of a clinical triad consisting of rapidly increasing myopia, normal axial length, and progressive axial subluxation leads to earlier diagnosis.[ncbi.nlm.nih.gov] A previously undescribed syndrome of bilateral blepharoptosis, ectopia lentis, and high myopia apparently was dominantly inherited and originated from a spontaneous genetic[ncbi.nlm.nih.gov]

  • Lens Dislocation

    . [3] Ocular diseases associated with ectopia lentis Simple ectopia lentis – simple ectopia lentis can occur as a congenital disorder or as a spontaneous disorder later in[eyewiki.aao.org] CONCLUSIONS: High myopia was the main risk factor for late in-the-bag IOL dislocation.[ncbi.nlm.nih.gov] CONCLUSION: The major predisposing factor for late in-the-bag IOL dislocation is myopia.[ncbi.nlm.nih.gov]

  • Marchesani-Weill Syndrome

    Simple dominant ectopia lentis. Pathogenic variants in FBN1 have been identified in some families. Inheritance is autosomal dominant. Ectopia lentis and pupilae.[ncbi.nlm.nih.gov] Abstract Objective: To describe the presenting features of Weill-Marchesani syndrome Case: A 22-year-old man presented with high myopia and progressive visual disturbance.[nepjol.info] Weill-Marchesani syndrome and secondary glaucoma associated with ectopia lentis.[ncbi.nlm.nih.gov]

  • Isolated Ectopia Lentis

    We here describe an isolated form of ectopia lentis in a large inbred family that shows autosomal-recessive inheritance.[ncbi.nlm.nih.gov] In addition to the well-known but inconstant displacement of the lens and pupil, other characteristics of this protean syndrome included severe axial myopia (and associated[jhu.pure.elsevier.com] Retinal function with lens‐induced myopia compared with form‐deprivation myopia in chicks Fujikado, T; Kawasaki, Y; Suzuki, A; Ohmi, G; Tano, Y.[deepdyve.com]

  • Disorder of the Lens

    . [3] Ocular diseases associated with ectopia lentis Simple ectopia lentis – simple ectopia lentis can occur as a congenital disorder or as a spontaneous disorder later in[eyewiki.aao.org] Nuclear cataract  index myopia., a previously ,ie presbyopic patient may be able to read again without the aid of spectacles.[slideshare.net] What is ectopia lentis syndrome?[marfan.org]

  • Foveal Hypoplasia - Presenile Cataract Syndrome

    Ectopia lentis may be hereditary or acquired.[archive.org] Impact of family history of high myopia on level and onset of myopia. Invest Ophthalmol Vis Sci. 2004;45(10):3446–3452. 11.[dovepress.com] lentis-chorioretinal dystrophy-myopia syndrome Endophthalmitis Endotheliitis Essential iris atrophy Familial benign flecked retina Familial congenital palsy of trochlear[se-atlas.de]

  • Lens Coloboma

    We present a case of Marfan syndrome with lens coloboma in one eye and ectopia lentis in the other. A 14-year-old girl reported decreased vision in the left eye.[ncbi.nlm.nih.gov] Trupti Shreyans Gadiya, Gunjan Ingle Purpose : To describe case of aniridia with ptosis, lens coloboma, myopia & foveal hypoplasia.[urbanedge.co.in] Bilateral ectopia lentis with isolated lens coloboma in Marfan syndrome Case Report Abstract A rare case of bilateral ectopia lentis with isolated lens coloboma in Marfan[egms.de]

  • Knobloch Syndrome Type 1

    In addition, six children had temporal ectopia lentis, found had posterior perinuclear lens opacity, two had developmental delay, one developed epilepsy, and one had heterotopic[cags.org.ae] Knobloch syndrome (KNO) is an autosomal recessive disorder characterized by ocular abnormalities (myopia and retinal detachment) and occipital encephalocele.[ncbi.nlm.nih.gov] ID Abbreviation Name OMIM ID Individuals Phenotypes Associated with genes Associated tissues Disease features 01764 - Ectopia lentis, isolated autosomal recessive 225100 16[databases.lovd.nl]

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