منابع مشابه
Hyperplasia of the adrenal medulla in hypertension of children.
Persistently high blood pressure is rare in childhood and warrants detailed investigation. Reviews on this subject by McCrory and Nash (1952) and Daeschner and Dodge (1959) have included extensive discussion of hormonal factors and adrenal tumours, but they make no mention of adrenal medullary hyperplasia. Adrenal medullary hyperplasia was found on histological examination in two children with ...
متن کاملAdrenal Medulla Autografts
In 1959, experiments were begun to provide a more physiological and permanent pacemaker for chronic heart block by placing an autotransplant of either adrenal medulla or thyroid gland into the ventricular myocardium of dogs with complete heart block. The original concept was that the small area of myocardium surrounding the endocrine transplant would be stimulated by relatively high local conce...
متن کاملCongenital Adrenal Hyperplasia and Schmid Metaphyseal Chondrodysplasia in a Child
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...
متن کاملa case of congenital lipoid adrenal hyperplasia
lipoid congenital adrenal hyperplasia (lipoid cah), a rare disorder of steroid biosynthesis, is the most severe form of cah. in this disorder the synthesis of glucocorticoids, mineralocorticoids and sex steroids is impaired which result in adrenal failure, severe salt wasting crisis and hyperpigmentation in phenotypical female infants irrespective of genetic sex. in this report, we presented a ...
متن کاملCongenital adrenal hyperplasia
Congenital adrenal hyperplasia consists of a heterogenous group of inherited disorders due to enzymatic defects in the biosynthetic pathway of cortisol and/or aldosterone. This results in glucocorticoid deficiency, mineralocorticoid deficiency, and androgen excess. 95% of CAH cases are due to 21-hydroxylase deficiency. Clinical forms range from the severe, classical CAH associated with complete...
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ژورنال
عنوان ژورنال: BMJ
سال: 1957
ISSN: 0959-8138,1468-5833
DOI: 10.1136/bmj.1.5012.186