Alport syndrome is a genetic disorder affecting around 1 in 5,000-10,000 children, characterized by glomerulonephritis, end-stage kidney disease, and... 23 KB (2,441 words) - 06:09, 16 November 2023 |
Type IV collagen (section Alport Syndrome) males. Mutations to the genes[COL4A5] coding for collagen IV lead to Alport syndrome. This will cause thinning and splitting of the glomerular basement... 21 KB (2,423 words) - 01:24, 21 April 2024 |
Epstein syndrome was first discovered in 1972 when two families had similar symptoms to Alport syndrome. Epstein syndrome and other Alport-like disorders... 17 KB (1,969 words) - 00:18, 12 March 2024 |
impairment should prompt a search for hereditary nephritis such as Alport syndrome.[citation needed] The molecular basis for thin basement membrane disease... 7 KB (762 words) - 21:22, 31 December 2023 |
syndrome Lenticonus posterior; lenticonus posterior is more common than lenticonus anterior and is sometimes found in Lowe syndrome Alport syndrome mostly... 3 KB (332 words) - 17:26, 30 May 2022 |
hypersensitivity syndrome Alopecia contractures dwarfism mental retardation syndrome Alpha-thalassemia mental retardation syndrome Alport syndrome Alström syndrome Alvarez'... 42 KB (4,155 words) - 22:50, 9 April 2024 |
Glomerulonephritis (section Nephrotic syndrome) nephrotic syndrome. This form of glomerulonephritis may be associated with conditions such as HIV and heroin abuse, or inherited as Alport syndrome. The cause... 21 KB (2,146 words) - 20:10, 12 January 2024 |
genetic disorders and hereditary diseases has been verified, including: Alport syndrome Colorectal cancer due to hereditary nonpolyposis colorectal cancer... 45 KB (3,828 words) - 11:36, 10 April 2024 |
IgA nephropathy (redirect from Berger's syndrome) causes of isolated hematuria include thin basement membrane disease and Alport syndrome, the latter being a hereditary disease associated with hearing impairment... 29 KB (3,482 words) - 14:50, 26 April 2024 |
syndrome is caused by a different mutation. For example, the vascular type (vEDS) of this disorder is caused by a mutation in collagen type 3. Alport... 64 KB (6,885 words) - 13:09, 20 April 2024 |
Samoyed breed of dog. The disease has been shown to be a model for Alport syndrome in humans in that the disease resembles that of the human disease.... 8 KB (963 words) - 19:11, 31 December 2023 |
retardation syndrome Alport syndrome Alport syndrome, dominant type Alport syndrome macrothrombocytopenia Alport syndrome, recessive type Alstrom's syndrome Alternating... 23 KB (1,929 words) - 03:48, 26 April 2024 |
PS (2003). "Cyclosporine A Slows the Progressive Renal Disease of Alport Syndrome (X-Linked Hereditary Nephritis): Results from a Canine Model". Journal... 23 KB (2,619 words) - 15:47, 3 March 2024 |
facial appearance, eye abnormalities, hearing loss, and joint problems. Alport syndrome – defects in collagen (type IV), found in the renal basement membrane... 12 KB (1,186 words) - 05:04, 25 February 2024 |
Manchester, England Alport syndrome, a genetic disorder Arthur Cecil Alport, the discoverer of Alport syndrome Cuthbert Alport, Baron Alport, a British politician... 697 bytes (107 words) - 14:48, 30 January 2019 |
Osteogenesis imperfecta (redirect from Cole carpenter syndrome) well as rare skeletal syndromes such as Bruck syndrome, hypophosphatasia, geroderma osteodysplasticum, and Ehlers–Danlos syndrome.: 1513 : 253–256 Various... 150 KB (15,363 words) - 22:39, 18 April 2024 |
basement membranes. Mutations in this gene are associated with X-linked Alport syndrome, also known as hereditary nephritis. Like the other members of the... 9 KB (1,020 words) - 09:17, 31 July 2023 |
Green's medical problems with anxiety and major hearing loss due to Alport syndrome. Green plays without any type of cymbals, instead replacing the usual... 4 KB (268 words) - 18:07, 15 December 2023 |
List of genetic disorders (redirect from List of genetic syndromes) RV, Turner S, Ledbetter DH, Martin CL (1993). "17q12 Recurrent Deletion Syndrome". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya... 42 KB (969 words) - 16:02, 3 April 2024 |
recessive), Treacher Collins syndrome (autosomal dominant), Crouzon syndrome (autosomal dominant), and Alport syndrome (X-linked). Other causes of congenital... 9 KB (1,236 words) - 21:22, 10 March 2024 |
Arthur Cecil Alport, M.D. (1880–1959) was a South African physician who first identified the Alport syndrome in a British family in 1927. After graduating... 4 KB (386 words) - 17:41, 9 February 2024 |
X-linked intellectual disability (redirect from Lindsay Burn syndrome) encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation". Genomics. 47 (3): 350–358... 18 KB (1,927 words) - 20:11, 28 January 2023 |