Sultan Al-Malki

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Congenital adrenal hyperplasia (CAH) owing to 21-hydroxylase deficiency is caused by the autosomal recessive inheritance of mutations in the gene CYP21A2. CYP21A2 mutations lead to variable impairment of the 21-hydroxylase enzyme, which, in turn, is associated with three clinical phenotypes, namely, salt wasting, simple virilizing, and nonclassical CAH.(More)
Patients with Congenital Adrenal Hyperplasia (CAH) owing to 21-hydroxylase deficiency and whose karyotype is 46, XX are usually assigned to the female gender. Reported herein are the long term outcomes in three patients with CAH whose karyotype is 46, XX and who were reared as males. A retrospective review of three CAH patients with a 46, XX karyotype who(More)
The prevalence and species distribution of Entamoeba histolytica and E. dispar in the Jadda region were studied. Data were collected by personal interview with all respondents over 5 years of age using a pre-designed questionnaire eliciting sociodemographic data such as age, sex, feeding health situation,education and environmental factors such as water(More)
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