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667 Possible Causes for Cataract, Hyperuricemia, Xeroderma

  • Diabetes Mellitus

    Considering this, we reviewed the principles and guidelines of managing cataract in patients with diabetes.[ncbi.nlm.nih.gov] Fructose is also the only sugar able to increase blood uric acid concentrations, and SSB consumption has been linked to development of hyperuricemia (serum uric acid level[doi.org] Hypothesis: fructose-induced hyperuricemia as a causal mechanism for the epidemic of the metabolic syndrome. Nat Clin Pract Nephrol. 2005 ; 1 : 80–86.[doi.org]

  • 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]

  • Chronic Kidney Insufficiency

    […] taking prednisone for long periods of time, these effects can be significant, including weight gain (especially around the face and trunk), moodiness, sleep disturbances, cataracts[kidshealth.org]

  • Cockayne Syndrome

    To describe cataracts in classic and early onset Cockayne syndrome (CS).[ncbi.nlm.nih.gov] After rehydration, allopurinol was commenced for her hyperuricemia.[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]

  • 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] […] combined 3 Calabro syndrome Familial glucocorticoid deficiency Chromosome 2q24 microdeletion syndrome Maffucci syndrome Autosomal dominant medullary cystic kidney disease with hyperuricemia[checkrare.com] 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]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    The ectodermal traits are clearly seen as trichodysplasia, onychodysplasia, skin manifestations, and nuclear cataract.[docslide.com.br] Other endocrine and metabolic abnormalities include hypothyroidism, diabetes insipidus, growth hormone deficiency, hyperuricemia, hyperlipidemia, hypothyroidism, and hypogonadotrophic[entokey.com] […] pigmentosum, group A XPA Xeroderma pigmentosum, group C XPC Xeroderma pigmentosum, group D ERCC2 Xeroderma pigmentosum, group E, DDB-negative subtype DDB2 Xeroderma pigmentosum[centogene.com]

  • Tricho-Retino-Dento-Digital Syndrome

    Nails Hair Hair: pili canaliculi uncombable hair pili trianguli Genitourinary External Genitalia Male: hypospadias Skeletal Feet: brachydactyly Head And Neck Eyes: juvenile cataract[malacards.org] Hyperthyroidism, Familial Gestational 2 Hyperthyroidism, Nonautoimmune 2 Hypertrichotic Osteochondrodysplasia 2 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 1 Hyperuricemia[preventiongenetics.com] […] hypohidrotic dysplasia Tricho retino dento digital syndrome Tricho-dento-osseous syndrome Tricho-hepato-enteric syndrome Trichodermodysplasia dental alterations Trichodysplasia xeroderma[mindmappedia.com]

  • Keratitis Bullosa

    Cornea and cataract. In: Emery, J.M.[link.springer.com] Hearing impairment Myelitis Abnormality of the ulna Raynaud phenomenon Abnormality of femur morphology Abnormality of tibia morphology Increased muscle glycogen content Hyperuricemia[mendelian.co] […] ou) Corneal Vascularisation DOUBLE PTERYGIUM OF LEFT EYE Melanin Granules on Corneal Endothelium (Krukenberg Spindle), (Colour Photography, OCT) Peripheral Degenerations Xeroderma[atlasophthalmology.net]

  • RAPADILINO Syndrome

    Complications include a high risk of skin cancer, with about half having skin cancer by age 10 without preventive efforts, and cataracts.[howlingpixel.com] […] combined 3 Calabro syndrome Familial glucocorticoid deficiency Chromosome 2q24 microdeletion syndrome Maffucci syndrome Autosomal dominant medullary cystic kidney disease with hyperuricemia[checkrare.com] […] photosensitivity) 0/14 0 41/41 100 25/25 100 Sparse scalp hair 0/14 0 15/30 50 3/5 50 Sparse brows or lashes 0/13 0 19/26 73 2/2 100 Radial ray defects c 14/14 100 8/40 20 3/5 67 Cataracts[doi.org]

  • Autosomal Recessive Primary Microcephaly Type 10

    Cataract MedGen UID: 368085 • Concept ID: C1962983 • Finding A cataract is an opacity or clouding that develops in the crystalline lens of the eye or in its capsule.[ncbi.nlm.nih.gov] Glioblastoma 3, 613029 ERBB2 Glioblastoma, somatic, 137800 TP53 Glioma susceptibility 1, 137800 PTEN Glioma susceptibility 2, 613028 UMOD Glomerulocystic kidney disease with hyperuricemia[gsdseq.ir] With Defects Of The Radius And Kidney Warburg Micro Syndrome 3 White Matter Hypoplasia-Corpus Callosum Agenesis-Intellectual Disability Syndrome Wolf-Hirschhorn Syndrome Xeroderma[familydiagnosis.com]

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