Work

Unmasking a rare variant: 17β-HSD3 deficiency in a male infant with disorders of sex development

Year: 2025

Type: article

Study design: Case Report

Source: BMJ Case Reports

DOI: 10.1136/bcr-2025-266828

Authors: Khadija Ali, Razan AR Abduljalil, Fatima Alqanea, Hussain Alsaffar

Institutions: King Hamad University Hospital, Sultan Qaboos University Hospital, University of Al-Ameed, Sultan Qaboos University

Language: English

Topic: Sexual Differentiation and Disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W4417427399

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Cites: 17

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