ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli +11 more
wiley +1 more source
Detecting Androgenetic Origin of the Genome via Single-Nucleotide Polymorphism-Based Cell-Free DNA Screening in Dichorionic Diamniotic Twin Pregnancies With Complete Hydatidiform Moles and a Coexisting Normal Fetus: A Three-Case Report. [PDF]
Yang YD +5 more
europepmc +1 more source
Case report: Fetomaternal hemorrhage-a lethal case and clinical insights for perinatal practice. [PDF]
Liu T, Guo S.
europepmc +1 more source
Establishment of an antepartum predictive model for postpartum hemorrhage in preterm delivery: a retrospective matched case-control study. [PDF]
Liao Q +6 more
europepmc +1 more source
Type C esophageal atresia masked by multiple overlapping causes of polyhydramnios in a monochorionic diamniotic twin pregnancy: A case report. [PDF]
Shima Y +4 more
europepmc +1 more source
Prevalence, risk factors, and adverse maternal and fetal outcomes of anemia during pregnancy: a retrospective study in China, 2012-2020. [PDF]
Liu X +11 more
europepmc +1 more source
Fetal anemia: Diagnosis and management
Fetal anemia has been known for many years as a dangerous complication of pregnancy. Its most common causes are maternal alloimmunization and parvovirus B19 infection, although it can be associated with many different pathological conditions including ...
Federico Prefumo +2 more
exaly +2 more sources

