The Association of Serum Level of TGF‐β1 and Clinical Manifestations in Sickle Cell Anemia: A Case‐Control Study

ABSTRACT Background and Aims Sickle cell anemia (SCA) is an inherited red blood cell disorder resulting from the polymerization of Hemoglobin S. Acute vaso‐occlusive crisis and multiple organ damage are the most common complications of SCA. Because of its multifunctional role in inflammation, endoth...

Full description

Saved in:
Bibliographic Details
Main Authors: Fatemeh Bakhshipour, Bita Bandar, Fatemeh Bineshfar, Najmeh Nameh Goshay Fard, Azar Babaahmadi, Najmaldin Saki, Kaveh Jaseb
Format: Article
Language:English
Published: Wiley 2025-07-01
Series:Health Science Reports
Subjects:
Online Access:https://doi.org/10.1002/hsr2.70960
Tags: Add Tag
No Tags, Be the first to tag this record!