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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.[] 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[] Hypothesis: fructose-induced hyperuricemia as a causal mechanism for the epidemic of the metabolic syndrome. Nat Clin Pract Nephrol. 2005 ; 1 : 80–86.[]

  • Hypoparathyroidism

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

  • 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[]

  • Cockayne Syndrome

    To describe cataracts in classic and early onset Cockayne syndrome (CS).[] After rehydration, allopurinol was commenced for her hyperuricemia.[] […] whose clinical presentation of cutaneous photosensitivity and central nervous system dysfunction is strongly reminiscent of the DeSanctis-Cacchione syndrome (DCS) variant of xeroderma[]

  • CAMFAK Syndrome

    Diseases related to Cataract, Microcephaly, Failure to Thrive, Kyphoscoliosis Syndrome via text searches within MalaCards or GeneCards Suite gene sharing: Human phenotypes[] […] combined 3 Calabro syndrome Familial glucocorticoid deficiency Chromosome 2q24 microdeletion syndrome Maffucci syndrome Autosomal dominant medullary cystic kidney disease with hyperuricemia[] He is also the Editor of Molecular Mechanisms of Fanconi Anaemia, Molecular Mechanisms of Xeroderma Pigmentosum, Molecular Mechanisms of Ataxia Telangiectasia and Molecular[]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

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

  • 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[] Hyperthyroidism, Familial Gestational 2 Hyperthyroidism, Nonautoimmune 2 Hypertrichotic Osteochondrodysplasia 2 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 1 Hyperuricemia[] […] hypohidrotic dysplasia Tricho retino dento digital syndrome Tricho-dento-osseous syndrome Tricho-hepato-enteric syndrome Trichodermodysplasia dental alterations Trichodysplasia xeroderma[]

  • Keratitis Bullosa

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

  • RAPADILINO Syndrome

    Complications include a high risk of skin cancer, with about half having skin cancer by age 10 without preventive efforts, and cataracts.[] […] combined 3 Calabro syndrome Familial glucocorticoid deficiency Chromosome 2q24 microdeletion syndrome Maffucci syndrome Autosomal dominant medullary cystic kidney disease with hyperuricemia[] […] 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[]

  • 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.[] Glioblastoma 3, 613029 ERBB2 Glioblastoma, somatic, 137800 TP53 Glioma susceptibility 1, 137800 PTEN Glioma susceptibility 2, 613028 UMOD Glomerulocystic kidney disease with hyperuricemia[] With Defects Of The Radius And Kidney Warburg Micro Syndrome 3 White Matter Hypoplasia-Corpus Callosum Agenesis-Intellectual Disability Syndrome Wolf-Hirschhorn Syndrome Xeroderma[]

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