Birthweight in Congenital Virilizing Adrenal Hyperplasia
نویسندگان
چکیده
منابع مشابه
Birthweight in congenital virilizing adrenal hyperplasia.
The deficiency of C-21-hydroxylation in adrenocorticosteroid synthesis is the commonest cause of congenital virilizing adrenal hyperplasia (CVAH). Abnormal secretory activity in CVAH begins about the third month of gestation before the differentiation of external genitalia (Bierich, 1963). The masculinization of the female external genitalia noted at birth in almost all cases is thought to resu...
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Isdale, J. M. (1970). Interstitial emphysema of the stomach. British journal of Radiology, 43, 146. Sisk, P. B. (1961). Gas in the portal venous system. Radiology, 77, 103. Susman, N., and Senturia, H. R. (1960). Gas embolization of the portal venous system. American j'ournal of Roentgenology, 83, 847. Touloukian, R. J., Berdon, W. E., Amoury, R. A., and Santulli, T. V. (1967). Surgical experie...
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Since it was shown by Wilkins et al. (1950) that high output of urinary 17-ketosteroids in cases of congenital virilizing adrenal hyperplasia was suppressed by administration of glucocorticoids, the syndrome has been considered to be due to a deficiency in the enzymatic processes necessary for biosynthesis of cortisol. The most common type of the cases shows disturbances in changing 17ƒ¿hydroxy...
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Congenital adrenal hyperplasia (CAH) is a group of hereditary diseases, which are autosomal recessive. CAH occurs due to defect in one of the cortisol coding genes and often clinically presents itself with signs of androgen overproduction. In this article, we report a case of CAH and Schmid metaphyseal dysplasia. Our literature review indicated that this report is the first attempt on CYP11B1 a...
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Deficiency of 21 hydroxylase enzyme deficiency (21OH) activity accounts for 90% cases of congenital adrenal hyperplasia (CAH). This results in deficient cortisol, increased ACTH, adrenal hyperplasia and increased adrenal androgen secretion. There is marked virilization in genetic females which is the hallmark of this disorder. Genetic heterogeneity in 21 OHD is well recognized, and both severe ...
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ژورنال
عنوان ژورنال: Archives of Disease in Childhood
سال: 1971
ISSN: 0003-9888,1468-2044
DOI: 10.1136/adc.46.247.350