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153 Possible Causes for Cataracts Usually Congenital, Congenital Eye Anomaly, Pediatric Disorder

  • Congenital Cataract

    What percentage of congenital cataracts are inherited and part of syndromes? Bilateral congenital cataracts are usually inherited or acquired?[quizlet.com] Evaluation of pediatric cataracts and systemic disorders. Curr Opin Ophthalmol. 2011; 22(5):365-79.[invitae.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]

  • 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] "Anterior Segment Disorders". Ruldolph’s Pediatrics. McGraw Hill Medical. pp. 2308-2313. (Good review of pediatric glaucoma, written for the pediatrician.)[clinicaladvisor.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]

  • 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] Detlef Bockenhauer and Robert Kleta, Renal Fanconi Syndromes and Other Proximal Tubular Disorders, Pediatric Kidney Disease, 10.1007/978-3-662-52972-0_32, (883-904), (2017[doi.org] Rena Okawa, Shuhei Naka, Kanae Saga and Kazuhiko Nakano, Lowe syndrome oral findings: Case report, Pediatric Dental Journal, 26, 1, (34), (2016).[doi.org]

  • Congenital Rubella Syndrome

    Congenital rubella syndrome is characterized by the triad of deafness, cataract and cardiovascular malformations.[ncbi.nlm.nih.gov] Oxytocin and autistic disorder: alterations in peptide forms. Biol Psychiatry. 2001 ; 50 : 609 – 613 American Academy of Pediatrics.[pediatrics.aappublications.org] .  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]

  • Congenital Eye Anomaly

    What Causes Congenital Cataracts? Cataracts clouding the eye's natural lens usually are associated with aging processes.[allaboutvision.com] It also may accompany a number of eye disorders and neurological disorders.[dmei.org] 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]

  • 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 Syphilis

    Progression of untreated congenital syphilis can result in meningitis, hydrocephalus, and cranial nerve injuries. Chorioretinitis and cataracts may develop.[clinicaladvisor.com] Pneumonia is common and usually occurs as bilateral fluffy infiltrates.[clinicaladvisor.com]

  • Late Congenital Syphilis

    Progression of untreated congenital syphilis can result in meningitis, hydrocephalus, and cranial nerve injuries. Chorioretinitis and cataracts may develop.[clinicaladvisor.com] Pneumonia is common and usually occurs as bilateral fluffy infiltrates.[clinicaladvisor.com]

  • Hallermann-Streiff Syndrome

    […] bilateral congenital cataracts, and microphthalmia.[profiles.uchicago.edu] Intended as a quick reference guide to the better known and some less familiar syndromes of neurological interest and developed by a renowned pediatric neurologist with more[books.google.com] 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]

  • 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]