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1,644 Possible Causes for Cataract, Xeroderma

  • Diabetes Mellitus

    Considering this, we reviewed the principles and guidelines of managing cataract in patients with diabetes.[ncbi.nlm.nih.gov] DIAGNOSES: The diagnoses of Diabetic cataracts, Type 1 diabetes and Diabetic retinopathy was made.[ncbi.nlm.nih.gov] Although acute diabetic cataracts are rarely encountered in clinical practice today, any rapidly maturing bilateral cortical cataracts in a child or young adult should alert[aao.org]

  • Ichthyosis Vulgaris

    PLATANUS OCCIDENTALIS 30 —Platanus occidentalis is prescribed for X linked ichthyosis with corneal opacity and cataract .[ks-gopi.blogspot.com]

  • Ichthyosis

    In a third in which the mother had cataracts and ichthyosis, two of her female children had cataracts.[disorders.eyes.arizona.edu] Ichthyosis, also called fish-skin disease, or xeroderma, a hereditary condition involving dryness and scaliness of the skin brought about by excessive growth of the horny[britannica.com] Types: xeroderma, xerodermia a mild form of ichthyosis characterized by abnormal dryness and roughness of the skin xeroderma pigmentosum a rare genetic condition characterized[vocabulary.com]

  • Hypoparathyroidism

    Abstract Cataract is a cardinal manifestation of hypoparathyroidism.[ncbi.nlm.nih.gov] […] leaded to increase the risk of cataract.[omicsonline.org] Signs and symptoms include muscle cramps, abdominal pain, dry skin, brittle nails, cataracts, tetany, and convulsions Condition produced by greatly reduced function of the[icd9data.com]

  • Cockayne Syndrome

    To describe cataracts in classic and early onset Cockayne syndrome (CS).[ncbi.nlm.nih.gov] […] whose clinical presentation of cutaneous photosensitivity and central nervous system dysfunction is strongly reminiscent of the DeSanctis-Cacchione syndrome (DCS) variant of xeroderma[ncbi.nlm.nih.gov] Xeroderma pigmentosum (XP)/Cockayne syndrome (CS) complex is a combination of clinical features of two rare genetic disorders in one individual.[ncbi.nlm.nih.gov]

  • Atopic Dermatitis

    After routine cataract surgery, the anterior subcapsular cataractous tissue was obtained as an anterior capsulorhexis flap and prepared as a wholemount for histological analysis[ncbi.nlm.nih.gov] Particularly, xeroderma pigmentosum patients are characterized by a 1,000-fold increased susceptibility to sunlight-induced skin cancer ( 4 ).[doi.org] All six patients had bilateral cataracts and cataract surgery was performed in eleven eyes. Bilateral simultaneous surgery was essential in two patients.[ncbi.nlm.nih.gov]

  • Cerebro-Oculo-Facio-Skeletal Syndrome Type 1

    Cerebro-oculo-facio-skeletal (COFS) syndrome is a rapidly progressive neurological disorder leading to brain atrophy with calcification, cataracts, microcornea, optic atrophy[ncbi.nlm.nih.gov] Inherited defects in NER result in profound photosensitivity and the cancer-prone syndrome xeroderma pigmentosum (XP) or two progeroid syndromes: Cockayne and trichothiodystrophy[ncbi.nlm.nih.gov] In many instances, the disorder results from a mutation in the Cockayne syndrome group B ( ERCC6/CSB ) gene or xeroderma pigmentosum (ie, DNA repair) genes ( ERCC2/XPD, ERCC5[medlink.com]

  • Rothmund Thomson Syndrome

    […] human disease Congenital poikiloderma RTS Rothmund-Thomson syndrome (disorder) ROTHMUND-THOMSON SYNDROME Poikiloderma Atrophicans and Cataract ROTHMUND-THOMSON SYNDROME; RTS[wikidata.org] The differential diagnosis should include other causes of childhood poikiloderma and other rare genodermatoses with prominent telangiectasias (including Bloom syndrome, xeroderma[orpha.net] Subscription Required Diagnostic Pearls Subscription Required Differential Diagnosis & Pitfalls Fanconi anemia Dyskeratosis congenita Ataxia-telangiectasia syndrome Bloom syndrome Xeroderma[visualdx.com]

  • Menopause

    […] working bladder and bowel Greater risk of Alzheimer's disease Poor skin elasticity (increased wrinkling) Poor muscle power and tone Some weakening in vision, such as from cataracts[webmd.com]

  • CAMFAK Syndrome

    Diseases related to Cataract, Microcephaly, Failure to Thrive, Kyphoscoliosis Syndrome via text searches within MalaCards or GeneCards Suite gene sharing: Human phenotypes[malacards.org] He is also the Editor of Molecular Mechanisms of Fanconi Anaemia, Molecular Mechanisms of Xeroderma Pigmentosum, Molecular Mechanisms of Ataxia Telangiectasia and Molecular[books.google.com] […] a nucleotide excision repair (NER) defect: xeroderma pigmentosum (XP), Cockayne syndrome (CS), and the photosensitive form of trichothiodystrophy (TTD).[ommbid.mhmedical.com]

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