Create issue ticket

308 Possible Causes for Low-Molecular-Weight Proteinuria

  • Oculocerebrorenal Syndrome

    […] tubular acidosis, aminoaciduria, and low-molecular-weight proteinuria.[en.wikipedia.org] Perinatal diagnosis may be achieved by detection of low molecular weight proteinuria. Diagnosis is confirmed by genetic screening of OCRL.[orpha.net] Oculocerebrorenal syndrome (also called Lowe syndrome ) is a rare X-linked recessive disorder characterized by congenital cataracts, hypotonia, intellectual disability, proximal[en.wikipedia.org]

  • Fanconi Syndrome

    The renal Fanconi syndrome is a defect of proximal tubular function causing aminoaciduria and low-molecular-weight proteinuria.[ncbi.nlm.nih.gov] All six displayed a novel phenotype of proximal tubulopathy, characterised by generalised aminoaciduria, low molecular weight proteinuria, glycosuria, hyperphosphaturia and[ncbi.nlm.nih.gov] The clinical features of FS are amino aciduria, low molecular weight proteinuria, hypophosphataemia, metabolic acidosis and glycosuria.[ncbi.nlm.nih.gov]

  • Acquired Fanconi Syndrome

    Treatment for Legionella pneumonia with antibiotics resulted in the improvement of all serum electrolyte abnormalities and normalization of the %TRP, FEK, FEUA, low-molecular-weight[ncbi.nlm.nih.gov] […] proximal tubular dysfunction include hypophosphatemia, hypouricemia and hypokalemia due to renal leakage, associated with normoglycemic glucosuria, generalized aminoaciduria, low-molecular-weight[orpha.net] In addition, hypokalemia, hypouricemia, metabolic acidosis and low-molecular-weight proteinuria can be part of the clinical spectrum [ 1 ].[bmcnephrol.biomedcentral.com]

  • Renal Tubular Dysfunction

    No study participants had low molecular weight proteinuria. Cellular mtDNA content in urine was heavily influenced by the cellularity of the sample.[ncbi.nlm.nih.gov] Abstract Low-molecular-weight (LMW) proteinuria has been described in patients with primary distal renal tubular acidosis (dRTA).[ncbi.nlm.nih.gov] Fanconi syndrome Damage to proximal tubular reabsorption of solutes, primarily glucose, amino acids, and phosphate; may also exhibit hypouricemia, proximal tubular acidosis, low-molecular-weight[accessmedicine.mhmedical.com]

  • Proteus

    […] of low-molecular-weight proteins (overflow).[amboss.com] […] the following: Amount of protein (nephrotic or non-nephrotic) Type of protein (albuminuria or low molecular weight proteinuria) Underlying pathological damage (glomerular[emedicine.medscape.com] Mixed proteinuria presents with glomerular and tubular protein fractions in urine, i.e., high- and low-molecular-weight proteins.[clinchem.aaccjnls.org]

  • Proteinuria

    We recommend the use of SDS-PAGE (sodium dodecyl sulfate electropheresis) for the detection of low molecular weight proteinuria.[ncbi.nlm.nih.gov] Dent disease is an X-linked proximal tubulopathy that typically presents with hypercalciuria, low-molecular-weight proteinuria and slow progression to endstage renal disease[ncbi.nlm.nih.gov] […] dysfunctional megalin causes the extremely rare Donnai-Barrow/Facio-Oculo-Acustico-Renal (DB/FOAR) syndrome characterized by a characteristic and multifaceted phenotype including low-molecular-weight[ncbi.nlm.nih.gov]

  • Focal Glomerulosclerosis

    The clinical diagnosis of Dent disease was established by intermittent hypercalciuria and low molecular weight proteinuria and confirmed through mutational analysis.[ncbi.nlm.nih.gov] […] careful diagnostic evaluation for possible underlying Dent disease should be considered in young boys who present with persistent albuminuria associated with high-grade low-molecular-weight[ncbi.nlm.nih.gov] It often manifests in childhood with symptoms of Fanconi syndrome and low-molecular-weight proteinuria.[ncbi.nlm.nih.gov]

  • Renal Stone

    Characteristics of the disease include low molecular weight proteinuria and hypercalciuria. Renal stones, nephrocalcinosis and renal failure often ensue.[mayo.edu] […] ultrasound, computed tomography, pathology and renal function , Pediatr Radiol , 1998 , vol. 28 (pg. 9 - 13 ) 24 Dent's disease; a familial proximal renal tubular syndrome with low-molecular-weight[academic.oup.com] molecular weight proteinuria with hypercalciuria and nephrocalcinosis) that we now know to be caused by defects in the same genetic locus on the X chromosome.[mayo.edu]

  • Distal Renal Tubular Acidosis

    Laboratory investigations revealed proximal tubular dysfunction (low molecular weight proteinuria, generalized hyperaminoaciduria, hypophosphatemia with hyperphosphaturia,[ncbi.nlm.nih.gov] Low-molecular-weight (LMW) proteinuria has been described in patients with primary distal renal tubular acidosis (dRTA).[ncbi.nlm.nih.gov] Education - 1978 Faculty of Medicine, The University of Tokyo Misc Renal cyst formation as a complication of primary distal renal tubular acidosis Nephron 59(1) 1991 Reversible low-molecular-weight[researchmap.jp]

  • Hereditary Late-Onset Parkinson Disease

    , LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS Contactin (K73/20) MYOPATHY, CONGENITAL, COMPTON-NORTH Copper Atpase 1 (L60/4) MENKES DISEASE, MILD CUTIS[neuromab.ucdavis.edu] SUSCEPTIBILITY TO GENERALIZED IDIOPATHIC EPILEPSY, TYPE 9 Clcn5 (N237/24) DENT DISEASE TYPE 1 NEPHROLITHIASIS, X-LINKED RECESSIVE HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE PROTEINURIA[neuromab.ucdavis.edu]

Further symptoms