Severe form of congenital adrenal hyperplasia caused by 11-β-hydroxylase deficiency in a 3-year old boy;Ciȩzka postać wrodzonego przerostu nadnerczy spowodowanego niedoborem 11-β-hydroksylazy u 3-letniego chlopca

Endokrynologia, Diabetologia i Choroby Przemiany Materii Wieku Rozwojowego

Volumn 6, Issue 2, 2000, Pages 151-156

  Starzyk, Jerzy ^a   Bartnik Mikuta, Anna ^a   Dziatkowiak, Hanna ^a  

^a JAGIELLONIAN UNIVERSITY MEDICAL COLLEGE   (Poland)

Author keywords

11 hydroxylase deficiency, precocious puberty

Indexed keywords

STEROID 11BETA MONOOXYGENASE;

ARTICLE; CASE REPORT; CLINICAL FEATURE; CONGENITAL ADRENAL HYPERPLASIA; DEVELOPMENTAL BIOLOGY; DISEASE COURSE; ENZYME DEFICIENCY; GROWTH RATE; HUMAN; MALE; PHYSICAL DEVELOPMENT; PRESCHOOL CHILD; PUBERTY; SEXUAL DEVELOPMENT;

EID: 17144459346     PISSN: 1234625X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (20)

1. The corticosteroid excretion pattern in infants and children with the adrenogenital syndrome
2. Congenital adrenal hyperplasia due to disorders of 11-beta-hydroxylation
3. Congenital adrenal hyperplasia with hypertension: Unusual steroid pattern in blood and urine
4. 19-Nor-deoxicorticosterone excretion in primary aldosteronism and low renin hypertension
5. Requirement of mineralocorticoid in congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
6. Salt loss in congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
7. Growth and pubertal development in patients with congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
8. Congenital adrenal hyperplasia in Turkey: A review of 273 patients
9. Acute adrenal crisis complicating hypertensive congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
10. Novel CYP11B1 mutation in congenital adrenal hyperplasia due to steroid 11 beta-hydroxylaze deficiency
11. Molecular pathology and mechanism of action of the steroidogenic acute regulatory protein, StAR
12. Hypertension in a neonete with 11 beta-hydroxylase deficiency
13. The NIH experience with precocious puberty: Diagnostic subgroups and response to short-term luteinizing hormone releasing hormone analogue therapy
14. Evidence for endocrinological abnormalities in heterozygotes for adrenal 11 beta-hydroxylaze deficiency of a family with R448H mutation in the CYP11B1 gene
15. High frequency of congenital adrenal hyperplasia (classic 11-beta-hydroxylase deficiency) among Jews from Marocco
16. Clinical variability of congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
17. A mutation in CYP11B1 (Arg-448-His) associated with steroid 11-beta-hydroxylase deficiency in Jews of Maroccan origin
18. Clinical and biochemical variability of congenital adrenal hyperplasia due to 11 beta-bydroxylase deficiency. A study of 25 patients
19. Salt loss in hypertensive form of congenital adrenal hyperplasia (11-beta-hydroxylase deficiency)