Hydrops Fetalis Latest Advances

Successful perinatal management of a large placental chorio-angioma: a case report demonstrating the effectiveness of a public-private partnership model.

Journal: Paediatrics and international child health

Published: January 20, 2026

A very rare cause of hydrops fetalis: idiopathic infantile arterial calcification.

Journal: Cardiology in the young

Published: January 19, 2026

Dehydrated hereditary stomatocytosis in 23 cases: a single-center retrospective cohort study from Peking Union Medical College Hospital (2018-2024)

Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi

Published: December 17, 2025

Isolated Transient Neonatal Ascites in a Preterm Infant Born to a Mother with Mirror Syndrome: A Case Report.

Journal: The American journal of case reports

Published: December 10, 2025

Defying the Odds: Survival in Severe Prenatal Caffey's Disease.

Journal: Cureus

Published: November 29, 2025

Predicting the Double Heterozygotes of HbE and α-Thalassemia-1 (Southeast Asian Type) Using RapidMiner-Generated Hematologic Algorithm.

Journal: Hemoglobin

Published: November 25, 2025

Maternal-fetal complications of non-immune fetal hydrops - mirror syndrome and hypereactio luteinalis with ovarian torsion: A case report.

Journal: Case reports in women's health

Published: November 25, 2025

A Clinical Practice Guideline for the Management of Pregnancy Alloimmunized to Red Blood Cell Antigens.

Journal: JAMA network open

Published: November 24, 2025

A Zika Virus-Like Particle Vaccine Mitigates Early Pregnancy Loss In Rhesus Macaques.

Journal: bioRxiv : the preprint server for biology

Published: November 24, 2025

Severe Hemolytic Disease of the Fetus Treated with Serial Intrauterine Transfusions: A Case Report and Review of Current Management.

Journal: Life (Basel, Switzerland)

Published: November 06, 2025

Transient Congenital Nephrotic Syndrome in Neonates: Two Case Reports and Review of Recent Literature.

Journal: Cureus

Published: October 16, 2025

Prenatal Imaging of Micrognathia, Micromelia, and Fetal Hydrops Leading to the Diagnosis of Achondrogenesis Type II with a COL2A1 Missense Mutation.

Journal: International journal of molecular sciences

Published: October 10, 2025