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1,426 Possible Causes for Hereditary Nephritis

  • Familial Interstitial Nephritis

    syndrome (AS) is rare; however, it does account for 3% of ESKD in childhood and is the most common of several types of hereditary nephritis.[patient.info] In patients with X-linked Alport syndrome, sensorineural hearing loss usually manifests in childhood, whereas renal disease often does not manifest until adulthood.[merckmanuals.com] We identified 150 patients with hereditary nephritis.[annals.org]

  • Alport Syndrome

    The mild form of hereditary nephritis described here was atypical for Alport's syndrome, but together with similar reports, suggests that a combination of May-Hegglin anomaly[ncbi.nlm.nih.gov] Abstract Hereditary nephritis with deafness, or Alport's syndrome, is a familial disorder characterized by progressive renal insufficiency, sensorineural hearing loss and[ncbi.nlm.nih.gov] Previous clinical studies only described epilepsy and EEG abnormalities in patients with hereditary nephritis (Alport syndrome).[ncbi.nlm.nih.gov]

  • Urinary Tract Infection

    Crossref Citations This article has been cited by the following publications. This list is generated based on data provided by CrossRef. Álvarez Lerma, F. Olaechea Astigarraga, P. Nuvials, X. Gimeno, R. Catalán, M. Gracia Arnillas, M.P. Seijas Betolaza, I. and Palomar Martínez, M. 2019. Is a project needed to prevent[…][doi.org]

  • Hypertension

    Abstract Background: It has long been known that depression is associated with hypertension but whether depression is a risk factor for hypertension incidence is still inconclusive. Objectives: To assess whether depression increases the incidence of hypertension. Method: Literatures were searched from PubMed,[…][doi.org]

  • Autosomal Dominant Macrothrombocytopenia

    Hereditary macrothrombocytopathia, nephritis and deafness. Am J Med 1972 ; 52 : 299 –310 2 Peterson LC, Rao KV, Crosson JT, White JG.[academic.oup.com] nephritis is rare; it is mainly included in a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly, Fechtner, Sebastian, Epstein and Alport syndrome[sjkdt.org] This is different from the Alport's syndrome, which consists of hereditary nephritis with deafness.[sjkdt.org]

  • Chronic Nephritis

    Abstract Forty-six patients from 23 Indian families with hereditary chronic nephritis (HCN) with or without Alport's syndrome are presented.[ncbi.nlm.nih.gov] Hereditary nephritis is a genetically heterogeneous disorder characterized by nephritic syndrome (ie, hematuria, proteinuria, hypertension, eventual renal insufficiency) often[merckmanuals.com] • Goodpasture’s Syndrome • Hereditary nephritis ( Alport’s Syndrome) Nephrotic syndrome • Amyloidosis • Diabetic nephropathy • Colagenic nephtopathy ( SLE scleroderma) Hematuric[intranet.tdmu.edu.ua]

  • Glomerulonephritis

    syndrome: Some studies have shown that there is an increased incidence of Chronic Glomerulonephritis in young males who have poor vision and poor hearing due to Alport syndrome[dovemed.com] Hereditary nephritis occurs in young men with poor vision and poor hearing.[healthline.com] Such individuals are thought to have a genetic predisposition to the condition (hereditary nephritis) Individuals having episodes of acute glomerulonephritis may develop the[dovemed.com]

  • Upper Airway Cough Syndrome

    syndrome Alports syndrome ; Hereditary nephritis; code to identify stage of chronic kidney disease (N18.1-N18.6) ICD-10-CM Diagnosis Code Q87.81 Alport syndrome 2016 2017[icd10data.com] […] upper eyelid L upper eyelid xanthelasma; Left upper xanthelasma ICD-10-CM Diagnosis Code H02.64 Xanthelasma of left upper eyelid 2016 2017 2018 2019 Billable/Specific Code Alport[icd10data.com]

  • Chronic Kidney Insufficiency

    Abstract Anemia is a major problem in patients with chronic kidney insufficiency. The development of recombinant human erythropoietin has enabled physicians to correct this anemia. Although anemia has not been considered to be a common or important contributor to congestive heart failure, anemia of any cause can[…][ncbi.nlm.nih.gov]

  • Hyperuricemia

    ., Alport syndrome ). Although rare individuals with ADTKD- UMOD have been found to have proteinuria, this is uncharacteristic.[ncbi.nlm.nih.gov] Autosomal-dominant chronic interstitial nephritis with early hyperuricemia.[ncbi.nlm.nih.gov] Hereditary nephropathy associated with hyperuricemia and gout. Arch Intern Med. 1993; 153 :357–65. [ PubMed : 8427538 ] Puig JG, Prior C, Martinez-Ara J, Torres RJ.[ncbi.nlm.nih.gov]

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