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179 Possible Causes for Cataracts Usually Congenital, Congenital Eye Anomaly

  • Congenital Cataract

    What percentage of congenital cataracts are inherited and part of syndromes? Bilateral congenital cataracts are usually inherited or acquired?[quizlet.com] Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 5 Walker-Warburg Syndrome Or Muscle-Eye-Brain Disease, FKRP-Related MDDGA5 613153[ukgtn.nhs.uk] Overview Background A cataract is an opacification of the lens. Congenital cataracts usually are diagnosed at birth.[emedicine.medscape.com]

  • Hallermann-Streiff Syndrome

    […] bilateral congenital cataracts, and microphthalmia.[profiles.uchicago.edu] Hallermann-Streiff syndrome is a rare congenital disorder characterized as a complex association of developmental anomalies involving structures of ectodermal origin (the[ncbi.nlm.nih.gov] The infant may also need to be treated for the inherited disorder that is causing the cataracts. Removing a congenital cataract is usually a safe, effective procedure.[medlineplus.gov]

  • Hypomyelinating Leukodystrophy Type 5

    The infant may also need to be treated for the inherited disorder that is causing the cataracts. Removing a congenital cataract is usually a safe, effective procedure.[medlineplus.gov] Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 5 Walker-Warburg Syndrome Or Muscle-Eye-Brain Disease, FKRP-Related MDDGA5 613153[ukgtn.nhs.uk] Hypomyelination and congenital cataract (HCC) is usually characterized by bilateral congenital cataracts and normal psychomotor development in the first year of life, followed[ncbi.nlm.nih.gov]

  • Ectopia Lentis

    Cataracts are by nature somewhat unpredictable but based upon location and etiology can usually be ascribed a predictive behavior; for instance, congenital nuclear cataracts[vin.com] Category Congenital malformation Brite Human diseases [BR: br08402 ] Congenital malformations Congenital malformations of eye H00662 Ectopia lentis Human diseases in ICD-11[genome.jp] Abstract Keratolenticular dysgenesis (KLD) and ectopia lentis are congenital eye defects.[ncbi.nlm.nih.gov]

  • Hydrophthalmos

    The hallmark of this disorder is the appearance of congenital bilateral cataracts (thick clouding of the lenses) that are usually deemed visually significant at birth.[news-medical.net] Megalocornea with glaucoma Q15.8 Other specified congenital malformations of eye Q15.9 Congenital malformation of eye, unspecified Inclusion term(s): Congenital anomaly of[icd10coded.com] The classical diagnostic triad includes: Congenital cataracts Neonatal or infantile hypotonia with subsequent mental impairment Renal tubular dysfunction progressing to chronic[patient.info]

  • Stickler Syndrome

    Abnormalities of vitreous gel architecture are a pathognomonic feature, usually associated with high myopia which is congenital and non-progressive.[ncbi.nlm.nih.gov] The vitreous showed distinct abnormalities consistent with congenital vitreous anomaly of type 1 Stickler syndrome.[ncbi.nlm.nih.gov] Features include: Ophthalmologic Congenital or early-onset cataracts.[en.wikibooks.org]

  • Congenital Malformation

    Four types of congenital cataracts, such as anterior polar, lamellar, polymorphic and total Red stethoscope and heart shape with plaster on it.[shutterstock.com] 740 Anencephalus and similar anomalies 741 Spina bifida 742 Other congenital anomalies of nervous system 743 Congenital anomalies of eye 744 Congenital anomalies of ear face[icd9data.com] Table 4 Frequency (and percentage of the total) of malformations by affected organ systems in subjects with multiple congenital anomalies.[bmcoralhealth.biomedcentral.com]

  • Oculocerebrorenal Syndrome

    The hallmark of this disorder is the appearance of congenital bilateral cataracts (thick clouding of the lenses) that are usually deemed visually significant at birth.[news-medical.net] The classical diagnostic triad includes: Congenital cataracts Neonatal or infantile hypotonia with subsequent mental impairment Renal tubular dysfunction progressing to chronic[patient.info] The diagnosis is initially suggested by uniformly present congenital cataract, while the recognition of cerebral manifestations is based on a comprehensive neurological examination[news-medical.net]

  • Lens Coloboma

    […] and Associated Systemic Diseases (see: Systemic Diseases) Congenital and Juvenile Cataracts, Usually Bilateral (see also: Congenital Syndromes) Anterior and Posterior Lenticonus[atlasophthalmology.net] Lens colobomas are congenital lens anomaly, rarely seen with Marfan syndrome. They are usually managed conservatively.[ncbi.nlm.nih.gov] Discussion Congenital anomalies of the lens are varied.[ijo.in]

  • Congenital Rubella Syndrome

    Congenital rubella syndrome is characterized by the triad of deafness, cataract and cardiovascular malformations.[ncbi.nlm.nih.gov] .  Rate of organ anomalies in CRS 5.  The classic triad for congenital rubella syndrome is:  Sensorineural deafness (58% of patients)  Eye abnormalities especially pigmentary[slideshare.net] […] manifesting in infancy, resulting from rubella infection in utero and characterized by signs or symptoms from the following categories: Cataracts/congenital glaucoma, congenital[deafblind.com]

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