Hypoxemia in thalassemia.

Southeast Asian J Trop Med Public Health

Thalassemia Center, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Published: May 1993

Data are reviewed describing hypoxemia, a newly identified feature in thalassemia. Evidence indicates platelet aggregation in the pulmonary circulation as being a key factor leading to hypoxemia and cor-pulmonale with right heart failure.

Download full-text PDF

Source

Publication Analysis

Top Keywords

hypoxemia thalassemia
4
thalassemia data
4
data reviewed
4
reviewed describing
4
describing hypoxemia
4
hypoxemia newly
4
newly identified
4
identified feature
4
feature thalassemia
4
thalassemia evidence
4

Similar Publications

Rationale: Mirror syndrome is a rare pregnancy condition in which maternal edema is associated with fetal hydrops. Because of its rarity and overlapping symptoms, this condition is often misdiagnosed as another pregnancy complication.

Patient Concerns: A 28-year-old pregnant Japanese woman presented with sudden 7.

View Article and Find Full Text PDF

Background: Renal tubular dysfunction is common in transfusion-dependent β thalassemia (β-TM). Iron overload, chronic anemia, and hypoxia are precipitating factors for renal insult. However, gut microbiota engagement in the renal insult has not been explored.

View Article and Find Full Text PDF

Dysregulation of macrophage polarization can prevent the invasion of trophoblast cells and further limit spiral artery remodeling in preeclampsia (PE). However, its mechanism is obscure. HTR8-/Svneo cells were cultured under normoxic or hypoxic conditions and extracellular vesicles (EVs) in the culture supernatants were extracted.

View Article and Find Full Text PDF

Genetic modifications of reactivate HbF production in β-thalassemia/HbE.

Heliyon

September 2024

Division of Clinical Microscopy, Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai, Thailand.

Article Synopsis
  • Reactivating fetal hemoglobin (HbF) has potential benefits for patients with β-thalassemia by improving their clinical symptoms.
  • Prolyl hydroxylase domain enzymes (PHDs), particularly PHD2, are important for oxygen sensing and maintaining the stability of HIF-α; inhibiting these enzymes can increase HbF production in cells.
  • Using CRISPR to modify PHD2’s functional regions resulted in lower PHD2 expression and higher HbF levels in severe β-thalassemia, highlighting a new regulatory mechanism that could be targeted for therapeutic purposes.
View Article and Find Full Text PDF

Infertility is a common issue that threatens couples worldwide. Infertility can result from the male or female partner alone, or both partners. It can be due to multiple factors related to the patient's overall health or lifestyle.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!