Cystic Hygroma
What's New
Last Posted: Mar 16, 2023
- Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China.
Yulin Zhou et al. Cytogenetic and genome research 2023 1-11 - Current Perspectives of Prenatal Cell-free DNA Screening in Clinical Management of First-Trimester Septated Cystic Hygroma.
Sherer David M et al. International journal of women's health 2022 141499-1518 - First Trimester Ultrasound in the Age of Cell-Free DNA Screening: What Are We Missing?
Ramdaney Aarti et al. Prenatal diagnosis 2022 - Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.
Sparks Teresa N et al. The New England journal of medicine 2020 Oct - Fetal Genetic Diagnosis by Chorionic Villus Sampling: Evaluation of the Five-Year Experience from a Single Center.
Öztürk Filiz Halici et al. Fetal and pediatric pathology 2020 Jan 1-9 - Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: update on genetic testing in the NGS era.
Stuurman Kyra E et al. Journal of medical genetics 2019 Apr - Cystic Hygroma: A Preliminary Genetic Study and a Short Review from the Literature.
Noia Giuseppe et al. Lymphatic research and biology 2018 Nov - Prenatal diagnosis of Down syndrome: A 13-year retrospective study.
Vicic Ana et al. Taiwanese journal of obstetrics & gynecology 2017 Dec 56(6) 731-735 - Cystic hygroma
From NCATS Genetic and Rare Diseases Information Center - Cystic hygroma lethal cleft palate
From NCATS Genetic and Rare Diseases Information Center - Fetal cystic hygroma
From NCATS Genetic and Rare Diseases Information Center
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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