[A novel homozygous variant in THSD1 causes non-immune hydrops fetalis in a premature infant].

Antenatal Diagnosis and Management of Congenital Pulmonary Airway Malformation: A Case Report.

Recurrent Male Hydrops Fetalis Reveals Hidden Incontinentia Pigmenti: Lessons From Pseudogene-Interfered Genomic Diagnosis.

Progressive non-immune hydrops fetalis associated with RASA1 mutation: prenatal imaging and genomic insights.

Neonatal management of parvovirus B19-induced hydrops fetalis: a case report.

Long-Segment Superior Vena Cava Hypoplasia as an Uncommon Cause of Non-immune Hydrops Fetalis.

Antenatal shunting and outcomes in fetuses with non-immune hydrops fetalis.

Mirror syndrome and placental ectopic liver in association with de novo SOS1 variant.

Genetic etiologies associated with non-immune hydrops fetalis delineated by whole exome sequencing: A pilot series and its implications in prenatal genetic counseling.

Non-Immune Hydrops Fetalis in a Pregnant Woman with Chronic Alcohol Use: A Case Report.

Dual pathology of parvovirus B19 infection and Aicardi-Goutières syndrome complicating non-immune hydrops fetalis.

Non-Immune Hydrops Fetalis, Multifocal Chorangiomatosis, and Noonan Syndrome 8.

Dual pathology of lower urinary tract obstruction and Brugada syndrome: A rare cause of non-immune hydrops fetalis.

Parvovirus B19 Infection in Pregnancy: Awareness of the Increased Incidence of Severe Intrauterine Infection.

Evaluation of Non-Immune Fetal Hydrops in Resource Poor Country: Challenges Faced in Ascertaining the Etiology.

Indications for fetal echocardiography: consensus and controversies among evidence-based national and international guidelines.

Whole Genome Sequencing in Prenatal Diagnostics: The Danish Approach to Guideline Formation and Implementation Within Public Healthcare.

Fetal Hydrops: Genetic Dissection of an Unspecific Sonographic Finding-A Comprehensive Review.

Mucopolysaccharidoses type VII (Sly syndrome): New uncertain pathogenic variants in GUSB gene.

Parvovirus B19 infection in children: a comprehensive review of clinical manifestations and management.

Case Report of Meconium Peritonitis: A Rare Cause of Non-immune Hydrops Fetalis.

Human parvovirus B19 vertical infection and hydrops fetalis. A case report.

Non-immune hydrops fetalis is associated with bi-allelic pathogenic variants in the MYB Binding Protein 1a (MYBBP1A) gene.

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.

Congenital metastatic neuroblastoma with placental involvement as a rare cause of non-immune fetal hydrops.

Congenital erythropoietic porphyria.

Disease characteristics, effectiveness, and safety of vestronidase alfa for the treatment of patients with mucopolysaccharidosis VII in a novel, longitudinal, multicenter disease monitoring program.

Syndromic and single gene disorders associated with fetal pleural effusion (I): Noonan syndrome, RASopathy and congenital lymphatic anomalies.

Chromosomal abnormalities associated with fetal pleural effusion (II): Specific and non-specific chromosome aberrations.

Chromosomal abnormalities associated with fetal pleural effusion (I): General overview.

Whole exome sequencing of a novel homozygous missense variant in PALB2 gene leading to Fanconi anaemia complementation group.

Clinical manifestations and genetic mutation analysis of patients with mucopolysaccharidosis type VII in China.

Prognostic indicators for long-term outcome of non-immune hydrops fetalis.

Novel premature termination codon in the FOXP3 gene as the cause of familial hydrops fetalis in males.

Mucopolysaccharidosis type VII (Sly syndrome) - What do we know?

Non-immune hydrops fetalis due to infantile sialidosis.

A de novo 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.

Resolving fetal hydrops - A rare entity.

Prenatal diagnosis of mucopolysaccharidosis type VII facilitating treatment in neonatal period.

PIEZO1 is the most common monogenic etiology of non-immune hydrops fetalis detected by prenatal exome sequencing.

Maternal outcomes of a cohort of pregnancies affected by non-immune hydrops fetalis.

Outcome and etiology of fetal pleural effusion, fetal ascites and hydrops fetalis after fetal intervention: retrospective observational cohort from a single institution.

Unique prenatal manifestations of biallelic NDUFAF5 variants: expansion of phenotype.

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.

Fetal Inferior Vena Cava Thrombosis Associated With Non-Immune Hydrops Fetalis and Maternal Mirror Syndrome.

Non-immune hydrops fetalis caused by Diamond-Blackfan anaemia and a mutation of the RPL15 gene.

Growth patterns in patients with mucopolysaccharidosis VII.

[Free sialic acid storage disorders with fetal hydrops in a neonate].

Fetal Homozygous GM1 Gangliosidosis Presenting as Transient Non-immune Hydrops Fetalis.

Genetic disorders and pregnancy outcomes of non-immune hydrops fetalis in a tertiary referral center.

The Cardiovascular Profile Score in Patients with Non-immune Hydrops Fetalis and Cardiac Anomalies - a Pilot Study.

Prenatal Clinical Findings in RASA1-Related Capillary Malformation-Arteriovenous Malformation Syndrome.

Diagnostic yield from prenatal exome sequencing for non-immune hydrops fetalis: A systematic review and meta-analysis.

An Investigation of the Etiologies of Non-Immune Hydrops Fetalis in the Era of Next-Generation Sequence-A Single Center Experience.

Recurrent Non-Immune Hydrops Fetalis: A Diagnostic Dilemma-"What to tell the Prospective Parents".

Perinatal presentations of non-immune hydrops fetalis due to recessive PIEZO1 disease: A challenging fetal diagnosis.

Human parvovirus B19 infection in a pregnant patient resulting in severe hydrops, foetal death and persistent infection.

A unique case of a newborn with a hemangioma on the omphalocele sac.

A case of non-immune hydrops fetalis with maternal mirror syndrome diagnosed by trio-based exome sequencing: An autopsy case report and literature review.

Prenatal diagnosis of non-immune hydrops fetalis: whole-exome sequencing or whole-genome sequencing?

A Gardos channelopathy associated with nonimmune hydrops and fetal loss.

Cost-Effectiveness of Exome Sequencing versus Targeted Gene Panels for Prenatal Diagnosis of Fetal Effusions and Non-Immune Hydrops Fetalis.

Isolated non-immune hydrops fetalis: an observational study on complete spontaneous resolution, perinatal outcome, and long-term follow-up.

Placental phenotype in non-immune hydrops fetalis with negative standard workup.

Diagnostic yield using whole-genome sequencing and in-silico panel of 281 genes associated with non-immune hydrops fetalis in clinical setting.

Non-immune hydrops fetalis caused by PIEZO1 compound heterozygous deletions detected only by exome sequencing.

Clinical Course and Outcome of Non-Immune Fetal Hydrops in Singleton Pregnancies.

Non-immune hydrops fetalis associated with two umbilical cord hemangiomas and vascular malformation of the transverse mesocolon. Case report.

[Whole exome sequencing analysis of compound heterozygous variants of CDAN1 gene in a Chinese family with non-immune hydrops fetalis].

Biallelic ANGPT2 loss-of-function causes severe early-onset non-immune hydrops fetalis.

An Atypical Case of Congenital Erythropoietic Porphyria.

Frequency and Prognosis of Hydrops Fetalis: A 10-Year Single-Center Experience.

Clinical Profile and Predictors of Mortality in Neonates Born With Non-Immune Hydrops Fetalis: Experience From a Lower-Middle-Income Country.

[Analysis of three families with recurrence of non-immune hydrops fetalis by trio whole exome sequencing].

Etiology and outcome of non-immune hydrops fetalis in relation to gestational age at diagnosis and intrauterine treatment.

Non-immune hydrops fetalis: Two case reports.

Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis.

Mucopolysaccharidosis VII in Brazil: natural history and clinical findings.

Value of Exome Sequencing in Diagnosis and Management of Recurrent Non-immune Hydrops Fetalis: A Retrospective Analysis.

Non-immune hydrops fetalis secondary to congenital chylothorax with diffuse interstitial lung disease: a diagnostic conundrum.

Fetal hydrops and the Incremental yield of Next-generation sequencing over standard prenatal Diagnostic testing (FIND) study: prospective cohort study and meta-analysis.

Neonatal hereditary spherocytosis caused by a de novo frameshift mutation of the SPTB gene characterized by hydrops fetalis: A case report.

Staged Management of Congenital Chylothorax With Hydrops Fetalis: An Insight Into EXIT Related Procedures.

Mucopolysaccharidosis type VII as a cause of recurrent Non-Immune Hydrops Fetalis: The first Tunisian case confirmed by Next-Generation Sequencing.

Fetal bradyarrhythmia causing hydrops fetalis: A journey from fetal echo to autopsy.

Identification of a homozygous deletion of the NEU1 gene in a patient with type II sialidosis presenting isolated fetal ascites and central nervous system hypoplasia.

Non-immune hydrops fetalis was rare in Sweden during 1997-2015, but cases were associated with complications and poor prognosis.

Non-immune Hydrops Fetalis and Hepatic Dysfunction in a Preterm Infant With Congenital Syphilis.

Pathway to diagnosis and burden of illness in mucopolysaccharidosis type VII - a European caregiver survey.

Infantile onset Pompe disease presenting with non-immune hydrops fetalis.

Etiology and Outcome of non-immune Hydrops Fetalis in Southern China: report of 1004 cases.

Diamond-Blackfan anemia RPL35A: a case report.

A Neonatal Case With Perinatal Lethal Gaucher Disease Associated With Missense G234E and H413P Heterozygous Mutations.

Early fetal hydropic changes are associated with moderate dilatation of the brain ventricular system: A clue to a possible link between cervical lymphatic engorgement and ventricular dilatation?

A system-based approach to the genetic etiologies of non-immune hydrops fetalis.

Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.

Non-immune hydrops fetalis neonate born to a mother with yellow nail syndrome.

Placental chorioangioma associated with polyhydramnios and hydrops fetalis.

Congenital erythropoietic porphyria: Recent advances.

A new case report of severe mucopolysaccharidosis type VII: diagnosis, treatment with haematopoietic cell transplantation and prenatal diagnosis in a second pregnancy.

No. 363-Investigation and Management of Non-immune Fetal Hydrops.

A recessive truncating variant in thrombospondin-1 domain containing protein 1 gene THSD1 is the underlying cause of nonimmune hydrops fetalis, congenital cardiac defects, and haemangiomas in four patients from a consanguineous family.

Coexistence of Kasabach-Merritt Syndrome and placental chorioangioma in a premature infant.

N° 363 - Évaluation et prise en charge de l'anasarque fœtoplacentaire non immune.

Generalized arterial calcification of infancy with a novel ENPP1 mutation: a case report.

Infection status of human parvovirus B19, cytomegalovirus and herpes simplex Virus-1/2 in women with first-trimester spontaneous abortions in Chongqing, China.

Thymic teratoma presenting as non-immune hydrops fetalis.

Metabolic causes of nonimmune hydrops fetalis: A next-generation sequencing panel as a first-line investigation.

Loss of function mutations in EPHB4 are responsible for vein of Galen aneurysmal malformation.

[Progress in genetic research on non-immune hydrops fetalis].

A case of vasculopathy of unknown etiology associated with fatal hydrops fetalis and review of the literature on intimomedial mucoid degeneration.

Non-immune hydrops fetalis: A retrospective analysis of 151 autopsies performed at a single center.

Non-Immune Hydrops Fetalis: Do Placentomegaly and Polyhydramnios Matter?

Inborn errors of metabolism in a cohort of pregnancies with non-immune hydrops fetalis: a single center experience.

Perinatal mortality in Japanese women diagnosed with gestational diabetes mellitus and diabetes mellitus.

LC-MS/MS multiplex analysis of lysosphingolipids in plasma and amniotic fluid: A novel tool for the screening of sphingolipidoses and Niemann-Pick type C disease.

Development of a new tandem mass spectrometry method for urine and amniotic fluid screening of oligosaccharidoses.

Archivée: Exploration et prise en charge de l'anasarque fœtoplacentaire non immune.

[NEW APPROACH IN DIAGNOSTIC ALGORITHM OF AN INFECTIOUS AGENTS (PARVOVIRUS B19 AND CHLAMYDIA TRACHOMATIS) INVOLVED IN THE DEVELOPMENT OF PATHOLOGICAL PREGNANCY].

A Rare Association of Non-Compaction of the Ventricular Myocardium, and Non-Immune Hydrops Fetalis.

Percutaneous umbilical blood sampling: current trends and outcomes.

Clinical course of sly syndrome (mucopolysaccharidosis type VII).

Perinatal and one-year outcomes of non-immune hydrops fetalis by etiology and age at diagnosis.

Congenital Disorder of Glycosylation (CDG) Presenting as Non-immune Hydrops Fetalis.

Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.

Perinatal-lethal Gaucher disease presenting as hydrops fetalis.

Relation between parvovirus B19 infection and fetal mortality and spontaneous abortion.

Maternal and fetal capillary malformation-arteriovenous malformation (CM-AVM) due to a novel RASA1 mutation presenting with prenatal non-immune hydrops fetalis.

Parvovirus B19 infection as a cause of acute myositis in an adult.

Non-immune Hydrops fetalis due to Parvovirus B19 Infection in 2 Extremely Preterm Infants: Perinatal Management and Long-term Neurodevelopmental Outcome.

Etiology of non-immune hydrops fetalis: An update.