Fetal Cystic Hygroma Latest Advances

Genetic and Sonographic Insights into First-Trimester Fetal Cystic Hygroma: A Retrospective 30-Year Analysis Using 3D/4D Ultrasound and Cytogenetic Evaluation in Croatia (1993-2023).

Journal: Genes

Published: July 18, 2025

Optical Genome Mapping for Prenatal Diagnosis in Fetuses With Structural Anomalies.

Journal: Prenatal diagnosis

Published: January 17, 2025

First-trimester application of non-invasive prenatal testing in the genetic investigation of fetal cystic hygroma and hydrops fetalis associated with Turner syndrome.

Journal: Taiwanese journal of obstetrics & gynecology

Published: October 25, 2024

A Novel NOTCH3 Variant Leading to Lateral Meningocele Syndrome: Prenatal Diagnosis and Possible Expansion of the Phenotype.

Journal: Molecular syndromology

Published: September 28, 2024

A cut-off value for nuchal translucency in the prediction of composite adverse outcome in cystic hygroma cases.

Journal: Revista da Associacao Medica Brasileira (1992)

Published: September 02, 2024

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?

Journal: Prenatal diagnosis

Published: July 27, 2023

Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygroma.

Journal: BMC medical genomics

Published: June 27, 2023

Fetal First-trimester Cystic Hygroma as the Prenatal Presenting Feature of ASCC1-Related Spinal Muscular Atrophy with Bone Fractures 2.

Journal: Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC

Published: May 03, 2023

A Placental Cyst Behind the Fetal Neck in the Mid-trimester Prenatal Sonography May Mimic a Fetal Cystic Hygroma.

Journal: Journal of medical ultrasound

Published: December 29, 2022

Retrospective analysis of genetic etiology and obstetric outcome of fetal cystic hygroma: A single-center study.

Journal: Medicine

Published: December 01, 2022

Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants.

Journal: Prenatal diagnosis

Published: August 30, 2022

Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China.

Journal: Cytogenetic and genome research

Published: August 29, 2022

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Genetic and Sonographic Insights into First-Trimester Fetal Cystic Hygroma: A Retrospective 30-Year Analysis Using 3D/4D Ultrasound and Cytogenetic Evaluation in Croatia (1993-2023).

Genetic and Sonographic Insights into First-Trimester Fetal Cystic Hygroma: A Retrospective 30-Year Analysis Using 3D/4D Ultrasound and Cytogenetic Evaluation in Croatia (1993-2023).

Optical Genome Mapping for Prenatal Diagnosis in Fetuses With Structural Anomalies.

Optical Genome Mapping for Prenatal Diagnosis in Fetuses With Structural Anomalies.

First-trimester application of non-invasive prenatal testing in the genetic investigation of fetal cystic hygroma and hydrops fetalis associated with Turner syndrome.

First-trimester application of non-invasive prenatal testing in the genetic investigation of fetal cystic hygroma and hydrops fetalis associated with Turner syndrome.

A Novel NOTCH3 Variant Leading to Lateral Meningocele Syndrome: Prenatal Diagnosis and Possible Expansion of the Phenotype.

A Novel NOTCH3 Variant Leading to Lateral Meningocele Syndrome: Prenatal Diagnosis and Possible Expansion of the Phenotype.

A cut-off value for nuchal translucency in the prediction of composite adverse outcome in cystic hygroma cases.

A cut-off value for nuchal translucency in the prediction of composite adverse outcome in cystic hygroma cases.

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?

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?

Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygroma.

Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygroma.

Fetal First-trimester Cystic Hygroma as the Prenatal Presenting Feature of ASCC1-Related Spinal Muscular Atrophy with Bone Fractures 2.

Fetal First-trimester Cystic Hygroma as the Prenatal Presenting Feature of ASCC1-Related Spinal Muscular Atrophy with Bone Fractures 2.

A Placental Cyst Behind the Fetal Neck in the Mid-trimester Prenatal Sonography May Mimic a Fetal Cystic Hygroma.

A Placental Cyst Behind the Fetal Neck in the Mid-trimester Prenatal Sonography May Mimic a Fetal Cystic Hygroma.

Retrospective analysis of genetic etiology and obstetric outcome of fetal cystic hygroma: A single-center study.

Retrospective analysis of genetic etiology and obstetric outcome of fetal cystic hygroma: A single-center study.

Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants.

Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants.

Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China.

Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China.