The Range of 2.2-3.3 mg/gCr of Pregnanetriol in the First Morning Urine Sample as an Index of Optimal Control in CYP21 Deficiency

Author:

Izawa Masako1,Aso Keiko1,Higuchi Asako1,Ariyasu Daisuke1,Hasegawa Yukihiro1

Affiliation:

1. Division of Endocrinology and Metabolism, Tokyo Metropolitan Kiyose Children's Hospital

Publisher

Japanese Society for Pediatric Endocrinology

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Reference11 articles.

1. 1. Paul MS. The adrenal cortex. In: Larsen PR, Kronenberg HM, Melmed S, Polonsky KS, editors. Wiliams textbook of endocrinology. 10th ed, Philadelphia: WB Saunders; 2002. p.491-551.

2. 3. Appan S, Hindmarsh PC, Brook CGD. Monitoring treatment in congenital adrenal hyperplasia. Arch Dis Child 1989;64:1235-9.

3. 4. Einaudi S, Lala R, Corrias A, Matarazzo P, Pagliardini S, Sanctis C. Auxological and biochemical parameters in assessing treatment of infants and toddlers with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Pediatr Endocrinol 1993;6:173-8.

4. 5. Bailey CC, Komrower GM, Palmer M. Management of congenital adrenal hyperplasia. Arch Dis Child 1978;53:132-5.

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1. Biochemical monitoring of 21-hydroxylase deficiency: a clinical utility of overnight fasting urine pregnanetriol;Current Opinion in Pediatrics;2024-05-31

2. Monitoring treatment in pediatric patients with 21-hydroxylase deficiency;Frontiers in Endocrinology;2023-02-03

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