• <em>PKD1L1</em> Is Involved in Congenital Chylothorax
• A <em>de novo</em> homozygous missense mutation of the GUSB gene leads to mucopolysaccharidosis type VII identification in a family with twice adverse pregnancy outcomes due to non-immune hydrops fetalis
• A novel variant in IFT122 associated with a severe phenotype of cranioectodermal dysplasia
• A rare hemoglobinopathy duo: Hb Adana×Hb SEA in a 1-year-old patient - a case report and a brief literature review
• A singleton pregnancy with placental chorioangioma and hydrops fetalis complicated with mirror syndrome and ritodrine-induced side effects: a case report
• Amniocentesis in pregnancies at or beyond 24 weeks: an international multicenter study
• An ongoing problem: Rhesus hemolytic disease of the newborn - A decade of experience in a single centre
• An Outbreak of Parvovirus B19 in Israel
• Analysis of complex chromosomal rearrangement involving chromosome 6 via the integration of optical genomic mapping and molecular cytogenetic methodologies
• Application of short tandem repeats (STRs) in the preimplantation genetic diagnosis (PGD) of α-thalassemia
• Approach to Pregnancy Affected by Kell Alloimmunization
• Autopsy case of linear nevus sebaceous syndrome with KRAS (G12D) mutation
• Biallelic truncating TTN variants in M-band encoding exons cause a fetal lethal titinopathy
• Causes of death in mucopolysaccharidoses
• Challenges of managing anomalous mitral arcade with severe mitral regurgitation and hydrops fetalis in infants
• Changing epidemiology of parvovirus B19 in the Netherlands since 1990, including its re-emergence after the COVID-19 pandemic
• Characterization of New Alpha Zero (α⁰) Thalassaemia Deletion (--^GB) among Malays in Malaysian Population
• Chromosomal abnormalities associated with fetal pleural effusion (I): General overview
• Chromosomal abnormalities associated with fetal pleural effusion (II): Specific and non-specific chromosome aberrations
• Clinical Management of Hydrops Fetalis in a Premature Neonate in India: A Case Report
• Clinical manifestations and genetic mutation analysis of patients with mucopolysaccharidosis type VII in China
• Comparing three cardiothoracic ratio measurement techniques and creating multivariable scoring system to predict Bart's hydrops fetalis at 17-22 weeks' gestation
• Congenital erythropoietic porphyria
• Congenital Erythropoietic Porphyria: A Rare Inherited Disorder
• Congenital metastatic neuroblastoma with placental involvement as a rare cause of non-immune fetal hydrops
• Congenital pulmonary lymphatic duct hypoplasia in a fetus with hydrops fetalis found at delivery: A case report
• Congenital tuberculosis causing hydrops fetalis: A case report and review of literature
• Correlation Between Ultrasonographic Placental Thickness and Adverse Fetal and Neonatal Outcomes
• Deciphering and disrupting PIEZO1-TMEM16F interplay in hereditary xerocytosis
• Dilatative fetal cardiomyopathy followed by a mirror syndrome
• Disease characteristics, effectiveness, and safety of vestronidase alfa for the treatment of patients with mucopolysaccharidosis VII in a novel, longitudinal, multicenter disease monitoring program
• Dual challenge inside the womb: a case report of concomitant fetal atrio-ventricular block associated with maternal anti-SSA antibodies and fetal tachyarrhythmia diagnosed as Wolff-Parkinson-White syndrome after birth
• Early prenatal diagnosis of causative homozygous variants in ASCC1 in a fetus with cystic hygroma and additional homozygous variants of unknown significance associated with a neurological phenotype not visible in early gestation: Dual diagnosis or not?
• Echocardiographic assessment of cardiovascular physiology of preterm miniature piglets supported with a pumped artificial placenta system
• Emergency Cesarean Section in a Dichorionic Diamniotic Twin Pregnancy With Hydrops Fetalis: A Report of a Critical Case
• Epidemic of parvovirus B19 and disease severity in pregnant people, Denmark, January to March 2024
• Etiology and perinatal outcomes between early and late-onset nonimmune hydrops fetalis
• Expansion of the prenatal phenotype of Baraitser-Winter syndrome: Presentation of two cases of multiple congenital anomaly syndrome
• Fetal bradyarrhythmias: classification, monitoring and outcomes of 40 cases at a single center
• Fetal cardiac teratoma and pericardiocentesis: A case report
• Fetal Hydrops Associated With 47,XXX: A Case Report and Literature Review
• Functional analysis of a novel splice site variant in the ASAH1 gene
• Glucose phosphate isomerase deficiency demasked by whole-genome sequencing: a case report
• Glucose-6-phosphate dehydrogenase deficiency as a cause for nonimmune hydrops fetalis and severe fetal anemia: A systematic review
• Haemoglobin Bart's Hydrops Fetalis: Charting the Past and Envisioning the Future
• Hemolytic Disease of the Fetus and Newborn
• Homozygous SPTA1-associated hereditary pyropoikilocytosis presenting as hydrops fetalis
• Hydrops fetalis caused by a complex congenital heart defect with concurrent hypoplasia of pulmonary blood vessels and lungs visualized by micro-CT in a French Bulldog
• Hydrops fetalis due to loss of function of hNav1.4 channel via compound heterozygous variants
• Identification of a Novel 16.8Kb Deletion of the α-Globin Gene Cluster by Third-Generation Sequencing
• Intrapericardial Teratoma and Associated 3q29 Deletion in a Fetus: Case Report
• Intrauterine transfusion in hydropic fetuses: An outcome analysis
• Large placental chorioangioma with maternal and perinatal morbidity
• Late third trimester diagnosis of congenital giant hemangioma complicated by the Kasabach-Merritt phenomen: a case report and literature review
• Lethal multiple pterygium syndrome, large cystic hygroma, and cleft palate: Rare and severe fetal presentations of RYR1- and NEB-related congenital myopathies
• Letter to the Editor: Management of Pregnancies Alloimmunized with Non-Rh and Non-K Alloantibodies
• Maternal isoimmunization associated fetal anemia: A case report
• Maternal outcomes of a cohort of pregnancies affected by non-immune hydrops fetalis
• Mechanosensation and lipid scrambling news
• Middle cerebral artery peak systolic velocity monitoring of fetal anemia during chemotherapy in pregnancy
• Mucopolysaccharidosis type VII (Sly syndrome) - What do we know?
• Multiple giant placental chorioangioma: A case report
• Neonatal pleural effusion associated with pulmonary sequestration: A case report
• Neonates with a prenatal diagnosis of hydrops fetalis: A 10-year experience in a tertiary care center
• Non-immune hydrops fetalis due to infantile sialidosis
• Nonimmune Hydrops and Left-Sided Cardiac Defect: Prenatal Presentation of Kabuki Syndrome
• Nonimmune Hydrops Fetalis
• Nonimmune Hydrops Fetalis
• Novel premature termination codon in the FOXP3 gene as the cause of familial hydrops fetalis in males
• Partial molar pregnancy with hydrops fetalis causing intrauterine fetal demise: A case report
• Parvovirus B19 in Pregnancy
• Perinatal Results and Long-Term Follow-Up of Fetal Cardiac Tumors: A 30-Year Historical Cohort Study
• Phenotypic heterogeneity associated with a novel MECOM variant: Mild thrombocytopenia to hydrops fetalis
• PIEZO Ion Channels in Cardiovascular Functions and Diseases
• PIEZO1 is the most common monogenic etiology of non-immune hydrops fetalis detected by prenatal exome sequencing
• Polycythemia revealing PIEZO1 hereditary xerocytosis
• Pregnancy outcomes of normal karyotype fetuses with increased nuchal translucency
• Prenatal and infantile diagnosis of craniosynostosis in individuals with RASopathies
• Prenatal Diagnosis and Postnatal Management of a Fetal Pericardial Mass
• Prenatal diagnosis of mucopolysaccharidosis type VII facilitating treatment in neonatal period
• Prenatal Management and Perinatal Outcome in a Large Series of Hydrops Fetalis
• Prenatal parvovirus B19 infection
• Prenatally Diagnosed Large Lung Lesions: Timing of Resection and Perinatal Outcomes
• Prognostic indicators for long-term outcome of non-immune hydrops fetalis
• Radiofrequency transcatheter ablation of the left lateral Kent bundle in a premature newborn after 28 weeks of pregnancy with prenatal diagnosis of incessant tachycardia: 28-year follow-up
• RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis
• Refractory supraventricular fetal tachycardia as a cause of non-immune hydrops: management conundrum
• Resolving fetal hydrops - A rare entity
• Retrospective study and implementation of a low-cost LAMP-turbidimetric assay for screening alpha(0)-thalassemia (SEA deletion): preventing and controlling Hb Bart's hydrops fetalis syndrome in Thailand
• Rh Incompatibility
• SAM domain variants of EPHB4 associated with aberrant signaling are linked to lymphatic-related fetal hydrops and facial dysmorphology
• Severe neuromuscular forms of glycogen storage disease type IV: Histological, clinical, biochemical, and molecular findings in a large French case series
• Severe Perinatal Presentations of Günther's Disease: Series of 20 Cases and Perspectives
• Single-tube multiplex real-time PCR with EvaGreen and high-resolution melting analysis for diagnosis of α0-thalassemia--SEA,--THAI, and--CR type deletions
• Spectrum of lymphatic anomalies in patients with RASA1-related CM-AVM
• Spontaneous regression of fetal pleural effusion in pregnancy complicated with Herpes simplex infection: Clinical presentation and literature review
• Syndromic and single gene disorders associated with fetal pleural effusion (I): Noonan syndrome, RASopathy and congenital lymphatic anomalies
• The role of fetal therapy in the management of mirror syndrome: a narrative review
• Viral-induced inflammation can lead to adverse pregnancy outcomes
• Whole exome sequencing of a novel homozygous missense variant in <em>PALB2</em> gene leading to Fanconi anaemia complementation group