Disease: Hydrops fetalis
- <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 diffuse, pustular eruption in a neonate: Recognizing SAMD9L-associated autoinflammatory disease (SAAD)
- A novel variant in IFT122 associated with a severe phenotype of cranioectodermal dysplasia
- A singleton pregnancy with placental chorioangioma and hydrops fetalis complicated with mirror syndrome and ritodrine-induced side effects: a case report
- 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
- Biallelic truncating TTN variants in M-band encoding exons cause a fetal lethal titinopathy
- Changing epidemiology of parvovirus B19 in the Netherlands since 1990, including its re-emergence after the COVID-19 pandemic
- Characterization of New Alpha Zero (α<sup>0</sup>) Thalassaemia Deletion (--<sup>GB</sup>) 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 features of fetal hydrothorax associated with mucopolysaccharidosis-VII
- 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: A Rare Inherited Disorder
- 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
- Cornelia de Lange Syndrome Presenting as Hydrops Fetalis due to Intestinal Atresia
- Correlation Between Ultrasonographic Placental Thickness and Adverse Fetal and Neonatal Outcomes
- Deciphering and disrupting PIEZO1-TMEM16F interplay in hereditary xerocytosis
- Diagnosis of α-thalassaemia by colorimetric gap loop mediated isothermal amplification
- Dual diagnosis of trisomy 21 and lethal perinatal Gaucher disease as a cause of non-immune hydrops fetalis in a twin pregnancy for a consanguineous couple
- 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?
- Emergency Cesarean Section in a Dichorionic Diamniotic Twin Pregnancy With Hydrops Fetalis: A Report of a Critical Case
- Epidemiology of birth defects based on a birth defects surveillance system in southwestern China and the associated risk factors
- Epidemiology of clinically significant forms of alpha- and beta-thalassemia: A global map of evidence and gaps
- Erythema Infectiosum
- Fetal Hemoglobin H Hydrops Fetalis: Another Three Case Reports
- Fetal Inferior Vena Cava Thrombosis Associated With Non-Immune Hydrops Fetalis and Maternal Mirror Syndrome
- First-trimester septated cystic hygroma, marked non-immune fetal hydrops, 45,X and coarctation of the aorta with neonatal survival
- Free sialic acid storage disorders with fetal hydrops in a neonate
- Functional analysis of a novel splice site variant in the ASAH1 gene
- Gaucher Disease
- Genetics, diagnostics and clinical presentation of primary lymphoedema
- Glucose phosphate isomerase deficiency demasked by whole-genome sequencing: a case report
- Growth patterns in patients with mucopolysaccharidosis VII
- Haemoglobin Bart's Hydrops Fetalis: Charting the Past and Envisioning the Future
- Homozygous SPTA1-associated hereditary pyropoikilocytosis presenting as hydrops fetalis
- Identification of a novel 91.5 kb-deletion (αα)<sup>FJ</sup> in the α-globin gene cluster using single-molecule real-time (SMRT) sequencing
- Intravenous immunoglobulin treatment of congenital parvovirus B19 induced anemia - a case report
- 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
- Low-frequency maternal novel MYH7 mosaicism mutation in recurrent fetal-onset severe left ventricular noncompaction: a case report
- Management of anti-M antibody during pregnancy: a case report
- Management of Pregnancies Alloimmunized with Non-Rh and Non-K Alloantibodies
- 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
- Mirror syndrome: a systematic literature review
- Molecular characterization of a novel 83.9-kb deletion of the α-globin upstream regulatory elements by long-read sequencing
- Mucopolysaccharidosis Type VII
- Mucopolysaccharidosis type VII (Sly syndrome) - What do we know?
- Multidisciplinary management of a large microcystic congenital pulmonary airway malformation: case report and literature review
- Neonates with a prenatal diagnosis of hydrops fetalis: A 10-year experience in a tertiary care center
- Non-immune hydrops fetalis caused by Diamond-Blackfan anaemia and a mutation of the RPL15 gene
- Non-immune hydrops fetalis due to infantile sialidosis
- Novel premature termination codon in the FOXP3 gene as the cause of familial hydrops fetalis in males
- Outcome and etiology of fetal pleural effusion, fetal ascites, and hydrops fetalis after fetal intervention: retrospective observational cohort from a single institution
- Partial molar pregnancy with hydrops fetalis causing intrauterine fetal demise: A case report
- Perinatal Outcomes of Fetuses with Prenatally Diagnosed Atrial Appendage Aneurysm
- 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
- Pregnancy outcomes of normal karyotype fetuses with increased nuchal translucency
- Prenatal and infantile diagnosis of craniosynostosis in individuals with RASopathies
- Prenatal diagnosis and early childhood outcome of fetuses with extremely large nuchal translucency
- 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
- 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
- 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
- Syndromic and single gene disorders associated with fetal pleural effusion (I): Noonan syndrome, RASopathy and congenital lymphatic anomalies
- Ten years' experience in prenatal diagnosis of α-thalassemia in a municipal hospital and retrospective analysis of ultrasonic abnormalities
- Thalassemia
- The role of fetal therapy in the management of mirror syndrome: a narrative review
- Two unrelated fetuses with ITPR1 missense variants and fetal hydrops
- Unique prenatal manifestations of biallelic NDUFAF5 variants: expansion of the phenotype
- 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