Reproductive Health in Women with Major β-Thalassemia: Evaluating Ovarian Reserve and Endocrine Complications

Reproductive Health in Women with Major β-Thalassemia: Evaluating Ovarian Reserve and Endocrine Complications

Thalassemia is an autosomal recessive hereditary chronic hemolytic anemia characterized by a partial or complete deficiency in the synthesis of alpha- or beta-globin chains, which are essential components of adult hemoglobin. Mutations in the globin genes lead to the production of unstable globin ch...

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Bibliographic Details
Main Authors: Vasileios Tsilionis, Efthalia Moustakli, Stefanos Dafopoulos, Athanasios Zikopoulos, Sotirios Sotiriou, Athanasios Zachariou, Konstantinos Dafopoulos
Format: Article
Language:English
Published: MDPI AG 2024-12-01
Series:Metabolites
Subjects:
hemoglobinopathies
HPG axis
reproductive endocrinology
ovarian biomarkers
reproductive health
infertility
Online Access:https://www.mdpi.com/2218-1989/14/12/717
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