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796 Possible Causes for Cataract, Progressive Liver Disease

  • Pneumonia

    […] convulsions 666 -- -- 1,029 -- 2,515 Non-malignant neoplasm 985 -- -- -- -- 1,566 Anemia and other deficiencies 1,262 -- -- 260* -- 1,704* Other urinary 875 -- -- 573 -- 1,067 Cataract[] The second type of K. pneumoniae causes a very severe form of the disease and is known as "hypervirulent." "The disease progresses very fast," Chen says.[] 8.7 2.4 6.2 4.9 Non-malignant neoplasm 1,375.22 9.6 9.7 0.3 1.0 0.0 Anemia and other deficiencies 2,520.79 6.7 8.9 0.4 5.5 16.6 Other urinary 718.65 5.8 6.3 2.1 5.1 0.4 Cataract[]

  • Endocrine Dysfunction

    Mutation in the nuclear-encoded mitochondrial isoleucyl-tRNA synthetase IARS2 in patients with cataracts, growth hormone deficiency with short stature, partial sensorineural[] With more advanced disease, a progressive fall in testosterone, leutinising hormone and triiodothyronine and a rise in oestradiol was observed.[] Severity of the liver disease determined by Child-Turcotte-Pugh class, rather than aetiology (alcoholic or postviral), was the chief determinant of such dysfunctions.[]

  • Wilson Disease

    病気 , 指定難病 上位クラス 肝障害 , metal metabolism disorder, copper metabolism disease, 器質性脳症候群, rare hereditary metabolic disease with peripheral neuropathy, metabolic disease with cataract[] Editorial Editorial More on this topic Progressive lenticular degeneration: a familial nervous disease associated with cirrhosis of the liver, by S. A.[] Kayser-Fleischer Ring and Sunflower Cataract in Wilson Disease . JAMA Ophthalmol. 2014 May 8. [Epub ahead of print].[]

  • Adrenal Insufficiency

    KEYWORDS: congenital cataracts; lactic acidosis; mitochondrial DNA (mtDNA) deletion; next generation panel[] Liver disease per se may lead to progressive impaired of HPA axis [ 9 ].[] PM (2.5-5.0 mg) Minor stress (symptoms of a cold or mild influenza) 30-50 mg/d PO in three divided doses Moderate stress (UTI, minor/moderate surgical procedure [such as cataract[]

  • Galactosemia

    Abstract A summary of the events occurring in galactose cataract is presented in Fig. 10.[] If an affected infant continues to drink milk the baby may develop symptoms that progress in days from jaundice, vomiting, and diarrhea, to liver disease and failure to thrive[] For infants or children with cataracts, galactosemia must be excluded.[]

  • Sterol 27-Hydroxylase Deficiency

    Cataract extraction is typically required by age 50 years. Cholic acid treatment has also been used.[] Notably, its deficiency causes a disease characterized by progressive neurologic impairment.[] ., is a rare by a deficiency in enzyme ceramidase which cause a progressive accumulation of fatty material lipids leading to abnormalities in the joints, liver, throat, tissues[]

  • Refsum Disease

    Findings included a noncorpuscular pigmentary degeneration of both fundi, optic nerve head drusen, attenuated retinal vasculature, cataract, myopia, and esotropia.[] […] of the disease.[] It causes retinitis pigmentosa, cataracts, a chronic polyneuropathy, cerebellar ataxia and cardiac arrhythmias amongst other clinical signs.[]

  • Hereditary Nephritis

    Ocular examination showed bilateral anterior lenticonus in 37.8%, retinal flecks in 22.2%, cataract in 20%, and keratoconus in 6.7% patients.[] MYH9RD is variably associated with young-adult onset of progressive sensorineural hearing loss, presenile cataract, elevation of liver enzymes, and renal disease manifesting[] Ocular examination showed bilat eral anterior lenticonus in 37.8%, retinal flecks in 22.2%, cataract in 20%, and keratoconus in 6.7% patients.[]

  • Diabetes Mellitus

    Considering this, we reviewed the principles and guidelines of managing cataract in patients with diabetes.[] […] steatohepatitis, and promote the progress of liver fibrosis.[] DIAGNOSES: The diagnoses of Diabetic cataracts, Type 1 diabetes and Diabetic retinopathy was made.[]

  • Fabry Disease

    Fabry cataract was recorded in 9.8% of females and in 23.1% of males.[] However, renal transplantation may not alter the course of disease progression in other organ systems.[] Affected mice were totally deficient in α-Gal A activity and progressively accumulated GL-3 in both plasma and the lysosomes of most tissues (in particular, the liver, spleen[]

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