Article
[Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia].
Orvosi hetilap - 1 Feb 2018
Doleschall Márton, Török Dóra, Mészáros Katalin, Luczay Andrea, Halász Zita, Németh Krisztina, Szücs Nikolette, Kiss Róbert, Tőke Judit, Sólyom János, Fekete György, Patócs Attila, Igaz Péter, Tóth Miklós
Abstract excerpt
Congenital adrenal hyperplasia is a group of genetic diseases due to the disablement of 7 genes; one of them is steroid 21-hydroxylase deficiency. The genes of congenital adrenal hyperplasia encode enzymes taking part in the steroidogenesis of adrenal gland. Steroid 21-hydroxylase deficiency is an autosomal recessive disorder caused by mutations of the steroid 21-hydroxylase gene. The mutations of steroid...
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