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887 Possible Causes for Juvenile Cataract

  • Rothmund Thomson Syndrome

    Recently we encountered a 25-year-old white woman who had developed this syndrome but without juvenile cataracts, hypogonadism, or mental retardation.[ncbi.nlm.nih.gov] Two clinical subforms of RTS have been defined: RTSI characterised by poikiloderma, ectodermal dysplasia and juvenile cataracts, and RTSII characterised by poikiloderma, congenital[ncbi.nlm.nih.gov] Rothmund-Thomson syndrome is a rare genodermatosis that features a progressive, early-onset poikiloderma, a high incidence of juvenile cataracts, stunted growth, and a wide[ncbi.nlm.nih.gov]

  • Cerebrotendinous Xanthomatosis

    We report the case of a child presenting with juvenile bilateral cataracts leading to the diagnosis of CTX.[ncbi.nlm.nih.gov] Pediatricians should be aware of this diagnostic possibility of cerebrotendinous xanthomatosis in children presenting with chronic diarrhea and juvenile cataracts.[ncbi.nlm.nih.gov] When affected children demonstrate lens opacities, ophthalmologists have the unique potential to facilitate earlier diagnosis and treatment by recognizing the juvenile cataract[ncbi.nlm.nih.gov]

  • Fabry Disease

    Fabry disease, also known as Anderson-Fabry disease, angiokeratoma corporis diffusum and alpha-galactosidase A deficiency, is a rare genetic lysosomal storage disorder. Some cases show no significant clinical manifestations. In other cases, the clinical manifestations of Fabrys disease appear early in life. With age,[…][symptoma.com]

  • Traumatic Cataract

    H26 Other cataract Excludes1 congenital cataract ( Q12.0 ) H26.0 Infantile and juvenile cataract H26.00 Unspecified infantile and juvenile cataract H26.001 Unspecified infantile[icd10coded.com] cataract H26.09 Other infantile and juvenile cataract H26.1 Traumatic cataract H26.10 Unspecified traumatic cataract H26.11 Localized traumatic opacities Reimbursement claims[icd10data.com] […] and Associated Systemic Diseases (see: Systemic Diseases) Congenital and Juvenile Cataracts, Usually Bilateral (see also: Congenital Syndromes) Intraocular Diseases, Cataracta[atlasophthalmology.net]

  • Congenital Cataract

    Nine other families have been previously reported with dominant congenital/juvenile cataracts and mutations in EPHA2.[ncbi.nlm.nih.gov] Back to top *Congenital and juvenile cataracts. Ophthalmology, 3rd ed . 2008. **Pediatric cataracts. Textbook of Family Practice, 7th ed. 2007.[allaboutvision.com] MAF mutations have been reported to cause juvenile-onset pulverulent cataract, microcornea, iris coloboma, and other anterior segment dysgenesis.[ncbi.nlm.nih.gov]

  • Turner Syndrome

    Turner syndrome (TS), also known as 45,X or 45,X0, is a condition in which a female is partly or completely missing an X chromosome. Signs and symptoms vary among those affected. Often, a short and webbed neck, low-set ears, low hairline at the back of the neck, short stature, and swollen hands and feet are seen[…][en.wikipedia.org]

  • Werner Syndrome

    The patient had a high-pitched voice, hoarseness, a characteristic bird-like facial appearance with a beak-shaped nose, canities and juvenile cataracts.[ncbi.nlm.nih.gov] Showing graying and loss of hair, skin atrophy, and juvenile cataract, he was diagnosed with Werner syndrome type 4 by molecular analysis.[ncbi.nlm.nih.gov] She displayed typical features of Werner syndrome including juvenile cataract, short stature and low weight, a bird-like face, a hoarse voice, and dry, atrophic, pigmented[ncbi.nlm.nih.gov]

  • Myotonic Dystrophy

    Myotonic dystrophy is a kind of multisystem disease, which is inherited in nature. It is a chronic disease condition that gradually progresses, causing muscle wasting, myotonia, heart defects and development of cataracts. Myotonic dystrophy significantly affects multiple organs and systems involving the skeletal[…][symptoma.com]

  • Laurence Moon Syndrome

    Synonyms: adipogenital-retinitis pigmentosa syndrome, LM syndrome This is a rare autosomal recessive condition. Laurence-Moon-Biedl syndrome and Laurence-Moon-Biedl-Bardet syndrome are no longer considered valid terms, because the patients of Laurence and Moon had paraplegia, but no polydactyly or obesity, which[…][patient.info]

  • Coronary Cataract

    According to Sautter in Velhagen's Der Augenarzt, the coronary cataract is classified under juvenile cataracts.[webeye.ophth.uiowa.edu] […] and Associated Systemic Diseases (see: Systemic Diseases) Congenital and Juvenile Cataracts, Usually Bilateral (see also: Congenital Syndromes) Anterior and Posterior Lenticonus[atlasophthalmology.net] Category: Cataract The patient was a 23-year-old Indian female.[webeye.ophth.uiowa.edu]

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