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1,012 Possible Causes for Cystic Kidney, Proteinuria

  • Fabry Disease

    It showed that the proteinuria emerged like surges, followed by temporary plasma GL-3 elevations in the early stages of classic Fabry disease.[] He suffered a relapse in proteinuria which responded to increased doses of the administered recombinant enzyme.[] […] with proteinuria.[]

  • Polycystic Kidney Disease

    Summary At present, there are no specific treatments available for patients with cystic kidney disease.[] Oxidized free Hcy and Cys with redox ratios were correlated to AOPP, MDA and proteinuria.[] […] of proteinuria.[]

  • Autosomal Dominant Polycystic Kidney Disease

    2015 ICD-9-CM Diagnosis Code 753.1 Cystic kidney disease There are 9 ICD-9-CM codes below 753.1 that define this diagnosis in greater detail.[] After 4 months, proteinuria decreased to 600 mg/d. Patients with ADPKD who show massive proteinuria should undergo kidney biopsy.[] Autosomal dominant polycystic kidney disease is one of the most prevalent forms of inherited cystic kidney disease, and can be characterized by kidney cyst formation and enlargement[]

  • Medullary Cystic Kidney Disease

    CYSTIC KIDNEY DISEASE 2; MCKD2 Medullary Cystic Kidney Disease type 2 MCKD2 Medullary Cystic Kidney Disease 2, Autosomal Dominant MEDULLARY CYSTIC KIDNEY DISEASE 2 Medullary[] Urinalysis showed occult hematuria and proteinuria(1.06 g/gCr). /β2- microglobulin 45,000 μg/ L, N-acetyl-/β-D-glucosaminidase 5.6 U/L.[] ADTKD should be suspected in patients with the following, particularly if the urinary sediment is benign: Polydipsia and polyuria Gout at a young age Proteinuria is absent[]

  • Nephronophthisis 1

    From Wikidata Jump to navigation Jump to search congenital disorder of urinary system medullary cystic kidney medullary cystic disease edit Language Label Description Also[] L) indicated predominantly tubular proteinuria.[] cystic disease kidney Medullary cystic disease of the kidney Medullary cystic kidney disease ICD-9-CM Volume 2 Index entries containing back-references to 753.16 :[]

  • Familial Interstitial Nephritis

    kidney disease 2 familial juvenile hyperuricaemic nephropathy uromodulin chromosome 16p gout Statistics from medullary cystic kidney disease 2 familial juvenile[] Lack of proteinuria, hematuria, hypertension, hyperuricemia, hearing loss, and visual impairment were present before the deterioration of the renal function.[] ) who have proteinuria with or without hypertension. [ 11 ] The addition of spironolactone to ACE-inhibitor treatment has been shown to reduce proteinuria significantly. [[]

  • Cystic Kidney

    SUMMARY: At present, there are no specific treatments available for patients with cystic kidney disease.[] […] contentious issue because the knowledge may evoke anxiety in terms of employment and insurance, screening of symptomatic cases or those that develop hypertension, hematuria and proteinuria[] […] tags Hearing loss Familial renal hamartomas Primary hyperparathyroidism Ossifying fibromas of the jaw Small to normal-sized kidneys Polydipsia and polyuria Absent-to-mild proteinuria[]

  • Autosomal Dominant Progressive Nephropathy with Hypertension

    Polycystic kidney, adult type Q61.3 Polycystic kidney, unspecified Q61.4 Renal dysplasia Q61.5 Medullary cystic kidney Q61.8 Other cystic kidney diseases Q61.9 Cystic kidney[] Alternatively, there may be no symptoms but urine shows erythrocytes, casts and proteinuria.[] Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy.[]

  • Nonallergic Interstitial Nephritis

    Injury Cryoglobuinemia Crystalglobulin-Induced Nephropathy Crystal-Induced Acute Kidney injury Cystic Kidney Disease, Acquired Cystinuria Dasatinib-Induced Nephrotic-Range[] Modest proteinuria and hyperkalemic renal tubular acidosis are common.[] Injury Cryocrystalglobulinemia Cryoglobuinemia Crystalglobulin-Induced Nephropathy Crystal-Induced Acute Kidney injury Crystal-Storing Histiocytosis Cystic Kidney Disease[]

  • Acute Renal Failure

    : e.g. angiomyolipoma Congenital defects Kidney duplication Cystic kidneys Horseshoe kidney Renal insufficiency (liable for hemodialysis if required) Uremia Acute renal failure[] Red blood cell casts, dysmorphic red cells, moderate to severe proteinuria TABLE 6 Findings on Urinalysis in the Broad Categories of Acute Renal Failure Type of renal failure[] Bushinsky -- Cystic kidney diseases / M. Amin Arnaout -- Hereditary nephropathies and developmental abnormaliteis of the urinary tract / Lisa M.[]

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