Germ Cell Dysfunction is Universal in Male Patients with β-Thalassemia Following Hematopoietic Stem Cell Transplantation During Childhood and Adolescence

Male patients with β-thalassemia after HSCT experienced universal impaired spermatogenesis and frequent Sertoli cell dysfunction but their Leydig cell function appeared to be preserved. Male patients and/or their guardians should be informed of the high likelihood of future subfertility before HSCT.

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Publication Details

Journal
Journal of Clinical Research in Pediatric Endocrinology
Published
2024-11-13
DOI
https://doi.org/10.4274/jcrpe.galenos.2024.2024-6-5
Citations
1
Primary Topic
Hemoglobinopathies and Related Disorders
Type
article
Field-Weighted Citation Impact
0.44
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article

Germ Cell Dysfunction is Universal in Male Patients with β-Thalassemia Following Hematopoietic Stem Cell Transplantation During Childhood and Adolescence

Wararat Chiangjong, Preamrudee Poomthavorn, Nuttha Piriyapokin, Pat Mahachoklertwattana et al.
1 citations
Journal of Clinical Research in Pediatric Endocrinology
Hemoglobinopathies and Related Disorders
0.44
article

Germ Cell Dysfunction is Universal in Male Patients with β-Thalassemia Following Hematopoietic Stem Cell Transplantation During Childhood and Adolescence

Wararat Chiangjong, Preamrudee Poomthavorn, Nuttha Piriyapokin, Pat Mahachoklertwattana, Usanarat Anurathapan
article en
1 citations

Abstract

Male patients with β-thalassemia after HSCT experienced universal impaired spermatogenesis and frequent Sertoli cell dysfunction but their Leydig cell function appeared to be preserved. Male patients and/or their guardians should be informed of the high likelihood of future subfertility before HSCT.

Journal of Clinical Research in Pediatric EndocrinologyVol. 17(2)
Mahidol University (TH), Ramathibodi Hospital (TH)
Openalex Percentile: Top 31%
Hemoglobinopathies and Related Disorders
0.44
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