2026-05-05T12:05:54Zhttps://uvadoc.uva.es/oai/request
oai:uvadoc.uva.es:10324/475022026-04-09T10:21:48Zcom_10324_32522com_10324_952com_10324_894col_10324_32523
UVaDOC author Rosado, Consolación author Bueno Martínez, Elena author Felipe, Carmen author Valverde, Sebastián author González Sarmiento, Rogelio 2021-07-19T06:14:29Z 2021-07-19T06:14:29Z 2015 Kidney and Blood Pressure Research, 2015, vol. 40, n. 4, p. 435-442 1420-4096 https://uvadoc.uva.es/handle/10324/47502 10.1159/000368519 435 4 442 Kidney and Blood Pressure Research 40 1423-0143 Background/Aims:Autosomal dominant Alport syndrome represents 5% of all Alport syndrome cases. This entity presents a different clinical expression from the recessive inheritance pattern and the X chromosome-linked pattern, because it is mild and it shows a late onset, which in many cases even goes unnoticed. Methods:We carried out a descriptive observational and retrospective clinical study on 19 patients from 5 families with a clinical diagnosis of autosomal dominant Alport Syndrome, and we analyzed the expression of the symptoms in the different families, comparing the results with what has been described in the literature. Results:Renal involvement appeared at a young age, with a progression towards end-stage chronic kidney disease at a median age of 31 years (20.5-36.5). Hearing involvement also appeared in early stages, at a median age of 28.5 years (7.5-62.5). Also, we observed ocular lenticonus-like injuries, which until now have only been described in other inheritance patterns. Conclusions:Our results suggest that dominant patterns are accompanied by a severe clinical expression that can be superimposed to the recessive and X chromosome-linked patterns, contrary to what has been classically stated. The high phenotypic variability observed in the families lead to the fact that many cases go unnoticed and the severest cases are erroneously diagnosed as recessive, which means that the real prevalence of dominant forms is probably higher than the current 5%. eng Attribution-NonCommercial-NoDerivatives 4.0 Internacional Study of the true clinical progression of autosomal dominant alport syndrome in a european population info:eu-repo/semantics/article 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URL https://uvadoc.uva.es/bitstream/10324/47502/1/Study-true-clinical-progression.pdf File MD5 28bfe66aceee5e037ca7a4336e7e2f44 913367 application/pdf Study-true-clinical-progression.pdf