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1,653 Possible Causes for Alport Syndrome

  • 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] - A dictionary of medical eponyms Related people Arthur Cecil Alport William Howship Dickinson The main characteristics of this very rare hereditary syndrome are progressive[whonamedit.com] Synonyms English : Alport Syndrome Alport Syndrome, Autosomal Dominant Alport Syndrome, Autosomal Recessive Alport Syndrome, X Linked Alport Syndrome, X-Linked Alport's Syndrome[decs.bvs.br]

  • High Myopia-Sensorineural Deafness Syndrome

    How is Alport Syndrome Diagnosed? How is Alport Syndrome Treated? Alport Syndrome Genetics and Inheritance Alport Syndrome Pathophysiology[news-medical.net] […] type 1 AD 180 561 COL4A3 Alport syndrome, Hematuria, benign familial AD/AR 123 264 COL4A4 Alport syndrome AD/AR 110 232 COL4A5 Alport syndrome XL 704 992 COL4A6 Deafness,[blueprintgenetics.com] Alport Syndrome Alport Syndrome is a group of hereditary kidney disorders.[tsbvi.edu]

  • Alport Syndrome

    Alport syndrome occurs in approximately 1 in 50,000 newborns. Mutations in the COL4A3, COL4A4, and COL4A5 genes cause Alport syndrome.[ghr.nlm.nih.gov] GeneReview/NIH/UW entry on Alport syndrome[en.wikipedia.org] Alport syndrome.[ncbi.nlm.nih.gov]

  • Goodpasture Syndrome

    syndrome.[nejm.org] syndrome was decreased, whereas epitope binding to heterologous antibodies recognizing all alpha3 NC1 epitopes remained the same.[ncbi.nlm.nih.gov] Mutations in genes corresponding to the building blocks of type IV collagen cause Alport's syndrome, whereas autoantibodies against structures that are usually hidden in the[nejm.org]

  • Renal Glomerular Disease

    Clinically, de novo anti-GBM disease in a recipient with X-linked Alport syndrome is characterized by the onset of a rapidly progressive GN.[cjasn.asnjournals.org] ., Alport syndrome).[what-when-how.com] syndrome/hereditary nephritis Fibrillary glomerulonephritis/immunotactoid glomerulopathy Paraproteinemias (amyloid/myeloma-related renal diseases) Clinical trials In addition[renal.wustl.edu]

  • Congenital Deafness

    In addition, the pattern of inheritance in the kindred was not consistent with X-linked Alport syndrome, since there was evidence of father-to-son transmission.[academic.oup.com] Most frequent syndromes related with genetic CD are the Alport Syndrome, the Brancio-Oto-Renal Syndrome, the X-linked dominant Charcot Marie Tooth disease, X-linked hereditary[symptoma.com] Alport syndrome Alport syndrome is caused by mutations in COL4A3, COL4A4 or COL4A5. These are genes that affect collagen.[dizziness-and-balance.com]

  • Glomerulonephritis

    syndrome.[ncbi.nlm.nih.gov] Alport syndrome. This is a form of inherited glomerulonephritis that affects both boys and girls. But boys are more likely to have kidney problems.[urmc.rochester.edu] […] types of GN were 95 IgA nephropathy, 47 focal segmental glomerulosclerosis, 14 membranous proliferative GN, 9 membranous GN, 8 lupus nephritis, 6 rapid progressive GN, and 4 Alport[ncbi.nlm.nih.gov]

  • Renal Hematuria

    When the usual suspects of urologic and glomerular causes of relatively isolated hematuria ( IgA nephropathy, Thin Basement Membrane Disease, Alport's Syndrome ) are not around[renalfellow.blogspot.com] Renal causes of hematuria include, but are not limited to, poststreptococcal glomerulonephritis, Alport syndrome, and thin basement membrane nephropathy.[texaschildrens.org] Hereditary nephritis (Alport syndrome), a progressive disorder that can be severe and lead to kidney failure and decreased hearing and vision.[merckmanuals.com]

  • Polymorphous Corneal Dystrophy

    Alport Syndrome is a hereditary disease that is caused by a gene mutation and affects the production of collagen in basement membranes; this condition causes hemorrhagic nephritis[ncbi.nlm.nih.gov] syndrome.[ncbi.nlm.nih.gov] Alport syndrome genetic renal disease extracellular matrix Introduction Alport syndrome is characterized by hematuria, progressive renal failure, hearing loss, and ocular[cjasn.asnjournals.org]

  • Nephrocalcinosis

    Alport syndrome Oxalosis Chronic glomerulonephritis Chronic transplant rejection[radipedia.com] syndrome and any other condition that disturbs the normal metabolism and distribution of calcium in the body.[symptoma.com] Causes of cortical nephrocalcinosis These include the following: Acute cortical necrosis Chronic glomerulonephritis Alport syndrome Prolonged hypercalcemia and/or hypercalciuria[emedicine.com]

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