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499 Possible Causes for Glycosuria, Proteinuria

  • Cystinosis

    All had nephropathic infantile-type cystinosis with evidence of proximal tubulopathy, with glycosuria and renal phosphate wasting.[] Based on the presence of parental consanguinity as well as polyuria, proteinuria, low tubular reabsorption of phosphorus, generalized aminoaciduria, light yellow skin and[] Diagnostic methods The diagnosis is based on blood and urine analysis showing features of Fanconi syndrome (metabolic acidosis, hypokalemia, hyperaminoaciduria, glycosuria[]

  • Fanconi Renotubular Syndrome 3

    Patients have polydipsia and polyuria with phosphaturia, glycosuria and aminoaciduria.[] Proteinuria dibedakan menjadi 2 yaitu, proteinuria fisiologis dan proteinuria patologis.[] Affiliated tissues include kidney and bone , and related phenotypes are proteinuria and metabolic acidosis[]

  • Cadmium Poisoning

    The effects of cadmium proximal renal function are characterized by increased cadmium in the urine, proteinuria (primarily Beta-2-microglobulin), aminoaciduria, glycosuria[] This so-called 'tubular proteinuria' is a good index of proximal tubular damage, but it is not usually detected by routine clinical dipstick testing for proteinuria.[] In the final stages of cadmium nephropathy, glycosuria, wasting of calcium and phosphate, and altered calcium metabolism with secondary effects on the skeleton of osteoporosis[]

  • Diabetes Mellitus

    Subsequently, hyperglycemia and glycosuria, but not ketonuria, occured.[] GI : gastroparesis in 25% of diabetics Renal : microalbuminuria- proteinuria- renal failure (delayed with ACE inhibitors or ARBs as well as BP control).[] Characteristically the course is progressive and includes polyuria, polydipsia, weight loss, polyphagia, hyperglycemia, and glycosuria.[]

  • Renal Vein Thrombosis

    The neonate was a macrosomic male born to a mother with glycosuria in pregnancy.[] By 3 weeks proteinuria disappeared completely and there was no reoccurrence of any proteinuria 4 months after discharge. Figure 1.[] .  Chronic Dramatic increase in proteinuria Evidence of tubule dysfunction Glycosuria Aminoaciduria Phosphaturia Impaired urinary acidification 10.  Definitive diagnosis[]

  • Acute Interstitial Nephritis

    Etiologically, renal glycosuria is of 3 types-benign renal glycosuria, glycosuria with diabetes mellitus (including gestational diabetes) and tubular defects (Fanconi syndrome[] Although her proteinuria was not heavy at the time of biopsy, her proteinuria subsequently increased to show nephrotic syndrome.[] Clinical features included acute kidney injury and proteinuria, but no sicca syndrome.[]

  • Acute Tubular Necrosis

    Glycosuria was documented in seven patients, five of whom were normoglycemic.[] Twenty-six patients (36%) required RRT a median of 4 (interquartile range, 2-6) days after detection of proteinuria and enzymuria.[] We therefore selected tubular proteinuria and enzymuria as logical markers in ATN.[]

  • Tyrosinemia Type 1

    Before starting NTBC therapy, all children manifested signs of renal dysfunction which included hypophosphatemia, acidosis, reduced phosphate reabsorption, aminoaciduria, glycosuria[] The severity of this disorder is variable and is typically characterized by tubular acidosis, aminoaciduria, glycosuria, and/or phosphaturia.[] Further laboratory tests (table 1)shows proteinuria , high level of serum Tyrosine and elevated level of succinylacetone so the diagnosis of late onset Tyrosinemia type 1[]

  • Oculocerebrorenal Syndrome

    Glycosuria. Lowe noted the absence of glycosuria in his first three patients, even when blood glucose levels were increased to 150 mg/dl in two patients ( 1 ).[] Renal function was assessed by measurements of proteinuria, urinary volume, and fractional excretions of potassium, phosphate, carnitine, and amino acids.[] A Hispanic girl with Lowe oculocerebrorenal syndrome (OCRL), an X-linked recessive condition characterized by cataracts, glaucoma, mental retardation, and proteinuria, is[]

  • Nephropathic Cystinosis

    Although hypoalbuminemia and massive proteinuria are characteristics of nephrotic syndrome, there are other conditions which can present with massive proteinuria.[] Proteinuria was present in all patients. Serum creatinine at last follow-up, without specific treatment, ranged between 69 and 450 mumol/L, at an age of 12 to 56 yr.[] Juvenile NC is associated with mild renal Fanconi syndrome or isolated proteinuria and manifests in childhood or adolescence.[]

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