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651 Possible Causes for Cataract, Hypomagnesemia, 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]

  • Hypoparathyroidism

    Abstract Cataract is a cardinal manifestation of hypoparathyroidism.[ncbi.nlm.nih.gov] Blood laboratory study results indicated serum hypocalcemia, hypomagnesemia, and hyperphosphatemia associated with a low parathyroid hormone level.[ncbi.nlm.nih.gov] […] awareness among physicians worldwide of this often unknown association, as life-threatening cardiac and neuromuscular complications can arise with unrecognized hypocalcemia and hypomagnesemia[ncbi.nlm.nih.gov]

  • Celiac Disease

    Increased risk of cataract among 28,000 patients with celiac disease. Am J Epidemiol. 2011 Jul 15. 174(2):195-202. [Medline]. Rosen A, Sandstrom O, Carlsson A, et al.[emedicine.com] The patient had normal anion-gap metabolic acidosis (pH   7.16) with persisting hypokalemia, hyponatremia, hypomagnesemia and hypophosphatemia.[ncbi.nlm.nih.gov] Electrolyte imbalances, such as low potassium level ( hypokalemia ), low calcium level (hypocalcemia), and low magnesium level (hypomagnesemia), may be present.[emedicinehealth.com]

  • Pellagra

    The oxidative damage led to rapid development of cataracts.[ncbi.nlm.nih.gov] Cataracts develop early, and to date none of the ten affected children has survived beyond 2 years of age.[ncbi.nlm.nih.gov] Cataracts Dietary vitamin B3, along with other nutrients is important for normal vision and prevention of cataracts (damage to the lens of the eye which can lead to cloudy[moyak.com]

  • Familial Isolated Hypoparathyroidism

    The clinical signs are mainly those of hypocalcemia: myopathy, muscular weakness, cramps, tetany, lenticular cataracts, teeth anomalies and short stature.[orpha.net] Congenital 2 with or without Brain or Eye Anomalies via MPDZ Gene Sequencing with CNV Detection ( #12013 ) Pediatric Cancer Sequencing Panel with CNV Detection ( #7973 ) Xeroderma[preventiongenetics.com] Main biochemical alterations Hypocalcemia, low or low-normal serum PTH levels, hyperphosphatemia, hypomagnesemia, high Ca/Cr ratio, low serum 1,25(OH)2 vitamin D.[iofbonehealth.org]

  • 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] […] syndrome Mohr-Tranebjaerg syndrome Shprintzen omphalocele syndrome X-linked lymphoproliferative syndrome 1 Potassium aggravated myotonia Spinocerebellar ataxia 29 Renal hypomagnesemia[checkrare.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] […] hypohidrotic dysplasia Tricho retino dento digital syndrome Tricho-dento-osseous syndrome Tricho-hepato-enteric syndrome Trichodermodysplasia dental alterations Trichodysplasia xeroderma[mindmappedia.com] 1, Intestinal 1 Hypomagnesemia 2, Renal 2 Hypomagnesemia 4, Renal 1 Hypomagnesemia 5, Renal, With Ocular Involvement 3 Hypomagnesemia 6, Renal 1 Hypomyelination And Congenital[preventiongenetics.com]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    The ectodermal traits are clearly seen as trichodysplasia, onychodysplasia, skin manifestations, and nuclear cataract.[docslide.com.br] […] 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] 1, Intestinal 1 Hypomagnesemia 2, Renal 2 Hypomagnesemia 4, Renal 1 Hypomagnesemia 5, Renal, With Ocular Involvement 3 Hypomagnesemia 6, Renal 1 Hypomyelination And Congenital[preventiongenetics.com]

  • Michels-Caskey Syndrome

    […] ataxia deafness Cataract congenital Volkmann type Cataract microcornea syndrome Cataract, total congenital Cataracts, ataxia, short stature, and mental retardation Catatrichy[rarediseases.info.nih.gov] X-linked severe combined immunodeficiency X-linked sideroblastic anemia X-linked susceptibility to autism-4 X-linked thrombocytopenia Xanthinuria type 1 Xanthinuria type 2 Xeroderma[rarediseases.info.nih.gov] 2 Renal hypomagnesemia-6 Renal hypouricemia Renal tubular acidosis with deafness Renal tubular acidosis, distal, autosomal dominant Renal tubulopathy, diabetes mellitus,[rarediseases.info.nih.gov]

  • Bagatelle-Cassidy Syndrome

    […] ataxia deafness Cataract congenital Volkmann type Cataract microcornea syndrome Cataract, total congenital Cataracts, ataxia, short stature, and mental retardation Catatrichy[rarediseases.info.nih.gov] X-linked severe combined immunodeficiency X-linked sideroblastic anemia X-linked susceptibility to autism-4 X-linked thrombocytopenia Xanthinuria type 1 Xanthinuria type 2 Xeroderma[rarediseases.info.nih.gov] 2 Renal hypomagnesemia-6 Renal hypouricemia Renal tubular acidosis with deafness Renal tubular acidosis, distal, autosomal dominant Renal tubulopathy, diabetes mellitus,[rarediseases.info.nih.gov]

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