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名词信息
中 文 名:
11-羟化酶缺陷症
英 文 名:
11-hydroxylase deficiency
中文又称:
中文曾称:
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所属专业:
内分泌科
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Pubmed相关的文献
11-hydroxylase deficiency
相关文献:
Challenges in treatment of patients with non-classic congenital adrenal hyperplasia.
Adriaansen BPH, Schröder MAM, Span PN, Sweep FCGJ, van Herwaarden AE, Claahsen-van der Grinten HL.
Front Endocrinol (Lausanne). 2022 Dec 12;13:1064024. doi: 10.3389/fendo.2022.1064024. eCollection 2022.
PMID:36578966
Treatment of Nonclassic 11-Hydroxylase Deficiency with Ashwagandha Root.
Powell D, Inoue T, Bahtiyar G, Fenteany G, Sacerdote A.
Case Rep Endocrinol. 2017;2017:1869560. doi: 10.1155/2017/1869560. Epub 2017 Jun 20.
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11-Hydroxylase deficiency as a cause of pre-pubertal gynecomastia.
Wasniewska M, Arrigo T, Lombardo F, Crisafulli G, Salzano G, De Luca F.
J Endocrinol Invest. 2009 Apr;32(4):387-8. doi: 10.1007/BF03345731.
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The uncommon forms of congenital adrenal hyperplasia.
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Congenital adrenal hyperplasia due to 11-hydroxylase deficiency-Compound heterozygous mutations of a prevalent and two novel CYP11B1 mutations.
Gu C, Tan H, Yang J, Lu Y, Ma Y.
Gene. 2017 Aug 30;626:89-94. doi: 10.1016/j.gene.2017.05.029. Epub 2017 May 14.
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Partial deficiency of adrenal 11-hydroxylase. A possible cause of primary hypertension.
de Simone G, Tommaselli AP, Rossi R, Valentino R, Lauria R, Scopacasa F, Lombardi G.
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Rare Types of Congenital Adrenal Hyperplasias Other Than 21-hydroxylase Deficiency.
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J Clin Res Pediatr Endocrinol. 2025 Jan 10;17(Suppl 1):23-32. doi: 10.4274/jcrpe.galenos.2024.2024-6-21-S. Epub 2024 Dec 23.
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A rare case of steroid 11 beta-hydroxylase deficiency in a child revealed by acute pulmonary edema.
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Congenital Adrenal Hyperplasias Presenting in the Newborn and Young Infant.
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The Rise, Fall, and Resurrection of 11-Oxygenated Androgens in Human Physiology and Disease.
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Horm Res Paediatr. 2018;89(5):284-291. doi: 10.1159/000486036. Epub 2018 May 9.
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