Create issue ticket

81 Possible Causes for Cataracts Usually Congenital, Congenital Eye Anomaly, Proteinuria

  • Oculocerebrorenal Syndrome

    The hallmark of this disorder is the appearance of congenital bilateral cataracts (thick clouding of the lenses) that are usually deemed visually significant at birth.[news-medical.net] The features of symptomatic Fanconi syndrome do not usually become manifest until after the first few months of life, except for LMW proteinuria.[ncbi.nlm.nih.gov] Renal function was assessed by measurements of proteinuria, urinary volume, and fractional excretions of potassium, phosphate, carnitine, and amino acids.[ncbi.nlm.nih.gov]

  • Congenital Cataract

    What percentage of congenital cataracts are inherited and part of syndromes? Bilateral congenital cataracts are usually inherited or acquired?[quizlet.com] Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 5 Walker-Warburg Syndrome Or Muscle-Eye-Brain Disease, FKRP-Related MDDGA5 613153[ukgtn.nhs.uk] Proteinuria, polyuria, as well as bicarbonate, sodium and potassium wasting with tubular acidosis are all part of the urinary profile.[disorders.eyes.arizona.edu]

  • Hydrophthalmos

    The hallmark of this disorder is the appearance of congenital bilateral cataracts (thick clouding of the lenses) that are usually deemed visually significant at birth.[news-medical.net] Megalocornea with glaucoma Q15.8 Other specified congenital malformations of eye Q15.9 Congenital malformation of eye, unspecified Inclusion term(s): Congenital anomaly of[icd10coded.com] Aminoaciduria, phosphaturia, calciuria, and proteinuria are present. Water resorption is impaired resulting in high volume and low osmolality.[patient.info]

  • Hypomyelinating Leukodystrophy Type 5

    The infant may also need to be treated for the inherited disorder that is causing the cataracts. Removing a congenital cataract is usually a safe, effective procedure.[medlineplus.gov] Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 5 Walker-Warburg Syndrome Or Muscle-Eye-Brain Disease, FKRP-Related MDDGA5 613153[ukgtn.nhs.uk] CLCN5 Hypophosphatemic rickets Sequencing of all coding exons of the gene - - 2.5 CLCN5 Nephrolithiasis, type I Sequencing of all coding exons of the gene - - 2.5 CLCN5 Proteinuria[cegat.de]

  • Stickler Syndrome

    Abnormalities of vitreous gel architecture are a pathognomonic feature, usually associated with high myopia which is congenital and non-progressive.[ncbi.nlm.nih.gov] The vitreous showed distinct abnormalities consistent with congenital vitreous anomaly of type 1 Stickler syndrome.[ncbi.nlm.nih.gov] Subsequent investigation identified low molecular weight proteinuria as part of their syndrome.[ncbi.nlm.nih.gov]

  • Cockayne Syndrome

    In 30% of cases, structural abnormalities of the eyes and early or congenital cataracts are present.[ijpd.in] Prenatal growth failure, congenital structural eye anomalies, severe neurologic dysfunction from birth, and the presence of cataracts within the first 3 years of life are[ncbi.nlm.nih.gov] However, the proteinuria intensified to become nephrotic syndrome. After 1 month the patient developed a gastric ulcer.[ncbi.nlm.nih.gov]

  • Congenital Malformation

    Four types of congenital cataracts, such as anterior polar, lamellar, polymorphic and total Red stethoscope and heart shape with plaster on it.[shutterstock.com] 740 Anencephalus and similar anomalies 741 Spina bifida 742 Other congenital anomalies of nervous system 743 Congenital anomalies of eye 744 Congenital anomalies of ear face[icd9data.com] The clinical significance of mild-grade proteinuria and hypertension seen in some patients is unknown [ 3 ].[patient.info]

  • Congenital Syphilis

    Progression of untreated congenital syphilis can result in meningitis, hydrocephalus, and cranial nerve injuries. Chorioretinitis and cataracts may develop.[clinicaladvisor.com] No recurrence of proteinuria was observed during the 1 year of follow-up.[ncbi.nlm.nih.gov] […] treated if infected [ Time Frame: 18 months ] Secondary Outcome Measures : The number of women who receive screening for other components of prenatal care (anemia, HIV, proteinuria[clinicaltrials.gov]

  • Late Congenital Syphilis

    Progression of untreated congenital syphilis can result in meningitis, hydrocephalus, and cranial nerve injuries. Chorioretinitis and cataracts may develop.[clinicaladvisor.com] […] hepatosplenomegaly (71%), rash (68%), Coombs-negative hemolytic anemia (58%), fever (42%), thrombocytopenia (40%), evidence of neurosyphilis (23%), pneumonitis (17%), renal involvement (proteinuria[clinicaladvisor.com] Pneumonia is common and usually occurs as bilateral fluffy infiltrates.[clinicaladvisor.com]

  • Renal Tubular Acidosis

    Lowe's syndrome — A rare inherited disorder that is distinguished by congenital cataracts, glaucoma, and severe mental retardation.[medical-dictionary.thefreedictionary.com] New Tests Hydrocephalus, Congenital 2 with or without Brain or Eye Anomalies via MPDZ Gene Sequencing with CNV Detection ( #12013 ) Pediatric Cancer Sequencing Panel with[preventiongenetics.com] The blood salicylate level was undetectable, and a urinalysis showed glycosuria, proteinuria and elevated beta-2 microglobulin and n-acetyl glucosamine levels, with a normal[ncbi.nlm.nih.gov]

Similar symptoms