Article

Successful live birth in women with partial 17α hydroxylase deficiency: report of two cases

2023-03-09

Abstract excerpt

<title>Abstract</title> <p><bold>Background: </bold>The condition 17αhydroxylase deficiency (17-OHD) is a rare kind of congenital adrenal hyperplasia (CAH) manifested by delayed sexual development, infertility, failure to synthetize cortisol, adrenal androgens and elevated progesterone (P4). Partial deficiency is much rarer, presenting with subtler symptoms. It can inhibit folliculogenesis, and affect endometrial...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: c5c7316b-63c5-5dab-b644-35d3b52c576b
DOI: 10.21203/rs.3.rs-2657814/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Successful live birth in women with partial 17α hydroxylase deficiency: report of two casesDOI 10.21203/rs.3.rs-2657814/v1Read

Successful live birth in women with partial 17α-hydroxylase deficiency: report of two casesSemantic proximity Read

Successful live birth in a Chinese woman with P450 oxidoreductase deficiency through frozen-thawed embryo transfer: a case report with review of the literatureSemantic proximity Read

Successful live birth in a Chinese woman with P450 oxidoreductase deficiency through frozen-thawed embryo transfer: a case report with review of the literatureSemantic proximity Read

Pregnancy in a Chinese woman with nonclassical 11β-hydroxylase deficiency caused by novel compound heterozygous mutations: a case report, literature review and functional validationSemantic proximity Read

Successful Live Birth in a Woman With 17α-Hydroxylase Deficiency Through IVF Frozen-Thawed Embryo Transfer.Semantic proximity Read

Assisted Reproduction in Congenital Adrenal HyperplasiaSemantic proximity Read

[Steroid 21-hydroxylase deficiencies and female infertility: pathophysiology and management].Semantic proximity Read

Partial 17alpha-hydroxylase/17,20-lyase deficiency-clinical report of five Chinese 46,XX cases.Semantic proximity Read

Severe Hyperandrogenism in 46,XX Congenital Adrenal Hyperplasia: Molecular Physiopathology, Late Diagnoses, and Personalized Management.Semantic proximity Read

Novel mutations of the CYP17A1 gene cause disorders of sex development in two-chromosome karyotype 46,XY infants and a literature review: A case reportSemantic proximity Read

Congenital Adrenal Hyperplasia with Combined 21-hydroxylase deficiency and 17α-hydroxylase/17,20-lyase deficiency: An undervirilized male.Semantic proximity Read

A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel MutationsSemantic proximity Read