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130 Possible Causes for Cataracts Usually Congenital, Congenital Eye Anomaly, Microphthalmos

  • Hallermann-Streiff Syndrome

    […] bilateral congenital cataracts, and microphthalmia.[profiles.uchicago.edu] The microphthalmos had overlapping posterior segment findings usually reported with Nanophthalmos and Posterior microphthalmos.[ncbi.nlm.nih.gov] 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]

  • 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] Signs : typically in the 6 o'clock position, often associated with other defects, eg microphthalmos, due to failed closure of optic fissure.Atypically in another position[vetstream.com] Lens colobomas are congenital lens anomaly, rarely seen with Marfan syndrome. They are usually managed conservatively.[ncbi.nlm.nih.gov]

  • Congenital Cataract

    […] short term of cataract surgery on microphthalmic eyes, in this prospective observational study we evaluated the long-term impact of bilateral cataract surgery on eyes with microphthalmos[clinicaltrials.gov] 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]

  • Congenital Eye Anomaly

    What Causes Congenital Cataracts? Cataracts clouding the eye's natural lens usually are associated with aging processes.[allaboutvision.com] . , , Source MeSH Eye Abnormalities Female Glaucoma, Open-Angle Humans Infant, Newborn Microphthalmos Umbilical Arteries Pub Type(s) Case Reports Comparative Study English[unboundmedicine.com] Congenital eye anomalies are an important cause of visual impairment in children worldwide, and are responsible for approximately 15–20% of blindness and severe visual impairment[nature.com]

  • Congenital Rubella Syndrome

    Congenital rubella syndrome is characterized by the triad of deafness, cataract and cardiovascular malformations.[ncbi.nlm.nih.gov] To describe a case of central serous chorioretinopathy after trabeculectomy surgery in an eye with microphthalmos in the setting of congenital rubella syndrome.[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]

  • 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] It is also the chromosomal abnormality most commonly associated with severe ocular defects, including microphthalmos, iris coloboma, and retinal dysplasia.[nature.com] 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]

  • 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] Q10.5 Congenital stenosis and stricture of lacrimal duct Q10.6 Other congenital malformations of lacrimal apparatus Q10.7 Congenital malformation of orbit Q11 Anophthalmos, microphthalmos[icd10data.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]

  • Peters Anomaly

    A family is described in which congenital cataracts with microcornea, and Peters' anomaly, appear to be variable expressions of a generalized anterior segment disorder inherited[ncbi.nlm.nih.gov] […] reports are described to illustrate the unusual occurrence of dominant inheritance of Peters' anomaly and the concomitant occurrence of Peters' anomaly with colobomatous microphthalmos[jhu.pure.elsevier.com] Category Congenital malformation Brite Human diseases [BR: br08402 ] Congenital malformations Congenital malformations of eye H01075 Peters anomaly Human diseases in ICD-11[genome.jp]

  • Microphthalmos

    The microphthalmos was seen in three forms: bilateral, severe or mild and severe microphthalmos of one eye with the fellow eye mildly affected.[ncbi.nlm.nih.gov] Other congenital diseases such as microcornea , microcoria , heterochromia iridis , microlentia , cataracts , retinal dysplasia , retinal detachment , anterior segment dysgenesis[vetbook.org] Four children with severe congenital eye anomalies are described of which three had related symptoms.[ncbi.nlm.nih.gov]

  • Congenital Muscular Dystrophy

    Clinical Characteristics Ocular Features: Cataracts have been diagnosed by 6 months of age and may be congenital in origin. Several patients have had strabismus.[disorders.eyes.arizona.edu] […] abnormalities such as crossed eyes (strabismus), cataracts, nearsightedness (myopia), abnormal eye movements, and, in severe cases, retinal detachment and abnormally small eyes (microphthalmos[rarediseases.org] (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13 Endo T.[ghr.nlm.nih.gov]