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94 Possible Causes for Recurrent Benign Hematuria Syndrome

  • Renal Pelvic Calculus

    2 cases of lesions of the dorsal renal artery in surgery for renal pelvic calculus are described. In 1 of the cases hypertension developed. Anatomic factors and previous operations predispose to this complication. An arterial complication should be suspected when hypertension develops postoperatively. The blood[…][ncbi.nlm.nih.gov]

  • Renal Hematuria

    […] familial hematuria – a genetic disorder causing persistent microscopic hematuria IgA nephropathy sickle cell trait or disease Alport syndrome – a genetic disorder causing[en.wikipedia.org] recurrent microscopic hematuria with proteinuria, hearing loss, and progressive kidney failure Diagnosis [ edit ] Sometimes the cause of hematuria can be determined based[en.wikipedia.org] […] hematuria in pediatric populations include: [12] hypercalciuria – suspected in a child with family history of kidney stones; can be asymptomatic or can cause painful urination benign[en.wikipedia.org]

  • IgA Glomerulonephritis

    Abstract The long pentraxin PTX3 has been recently involved in amplification of the inflammatory reactions and regulation of innate immunity. In the present study we evaluated the expression and role of PTX3 in glomerular inflammation. PTX3 expression was investigated in the IgA, type I membranoproliferative, and[…][ncbi.nlm.nih.gov]

  • Familial Hypercholesterolemia

    1 Behr Syndrome 1 Benign Familial Hematuria 1 Benign Familial Neonatal Seizures 1 1 Benign Familial Neonatal-Infantile Seizures 2 Benign Hereditary Chorea 1 Benign Recurrent[preventiongenetics.com] Basal Ganglia Calcification, Idiopathic, 6 1 Basal Ganglia Disease, Biotin-Responsive 4 Basel-Vanagait-Smirin-Yosef Syndrome 1 Becker Muscular Dystrophy 3 Beckwith-Wiedemann Syndrome[preventiongenetics.com]

  • Uremic Pneumonitis

    ) Benign recurrent hematuria (thin BM disease) Alport's syndrome (hereditary nephritis) nephritis accompanied by nerve deafness and various eye disorders due to a mutation[studyblue.com] […] nephropathy LM: "Collapsing glomerulopathy" - shrunken in Bowman's space, epithelial hyperplasia EM: reticulotubule inclusions, granular change Hereditary nephritis (Alport's syndrome[studyblue.com]

  • Dilated Cardiomyopathy Type 2B

    1 Behr Syndrome 1 Benign Familial Hematuria 1 Benign Familial Neonatal Seizures 1 1 Benign Familial Neonatal-Infantile Seizures 2 Benign Hereditary Chorea 1 Benign Recurrent[preventiongenetics.com] Basal Ganglia Calcification, Idiopathic, 6 1 Basal Ganglia Disease, Biotin-Responsive 4 Basel-Vanagait-Smirin-Yosef Syndrome 1 Becker Muscular Dystrophy 3 Beckwith-Wiedemann Syndrome[preventiongenetics.com]

  • Lipoid Nephrosis

    Fibrin was generally absent in lipoid nephrosis in remission and in benign recurrent hematuria.[ncbi.nlm.nih.gov] Fibrin and platelets were also found in cases of nephrotic syndrome due to other causes, and in glomerulonephritis.[ncbi.nlm.nih.gov]

  • Other Primary Thrombocytopenia

    1 Behr Syndrome 1 Benign Familial Hematuria 1 Benign Familial Neonatal Seizures 1 1 Benign Familial Neonatal-Infantile Seizures 2 Benign Hereditary Chorea 1 Benign Recurrent[preventiongenetics.com] Basal Ganglia Calcification, Idiopathic, 6 1 Basal Ganglia Disease, Biotin-Responsive 4 Basel-Vanagait-Smirin-Yosef Syndrome 1 Becker Muscular Dystrophy 3 Beckwith-Wiedemann Syndrome[preventiongenetics.com]

  • Gingival Fibromatosis-Progressive Deafness Syndrome

    1 Behr Syndrome 1 Benign Familial Hematuria 1 Benign Familial Neonatal Seizures 1 1 Benign Familial Neonatal-Infantile Seizures 2 Benign Hereditary Chorea 1 Benign Recurrent[preventiongenetics.com] Basal Ganglia Calcification, Idiopathic, 6 1 Basal Ganglia Disease, Biotin-Responsive 4 Basel-Vanagait-Smirin-Yosef Syndrome 1 Becker Muscular Dystrophy 3 Beckwith-Wiedemann Syndrome[preventiongenetics.com]

  • Laron Syndrome with Immunodeficiency

    10 Behr Syndrome 5 Benign Familial Hematuria 3 Benign Familial Neonatal Seizures 1 2 Benign Familial Neonatal-Infantile Seizures 3 Benign Hereditary Chorea 1 Benign Recurrent[preventiongenetics.com] […] autosomal recessive 1 Basal Ganglia Disease, Biotin-Responsive 7 Basal Laminar Drusen 1 Basel-Vanagait-Smirin-Yosef Syndrome 2 Becker Muscular Dystrophy 5 Beckwith-Wiedemann Syndrome[preventiongenetics.com]

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