Cystic hygroma and non-immune hydrops fetalis

2007 ◽  
pp. 103-111
Keyword(s):  
Cystic Hygroma ◽  
Hydrops Fetalis

scholarly journals Severe cystic hygroma and hydrops fetalis in a Turner's syndrome

2016 ◽  
Vol 206 ◽  
pp. e20
Author(s):  
Cristina Bragança ◽  
Lara Caseiro ◽  
Fausto Barata ◽  
Maria José Janeiro
Keyword(s):  
Cystic Hygroma ◽  
Hydrops Fetalis ◽  
Turner's Syndrome ◽  
Turner’S Syndrome

Cystic hygroma and hydrops fetalis in a fetus with trisomy 13

1983 ◽  
Vol 24 (5) ◽  
pp. 389-391 ◽  
Author(s):  
Frank Greenberg ◽  
Robert J. Carpenter ◽  
David H. Ledbetter
Keyword(s):  
Cystic Hygroma ◽  
Hydrops Fetalis ◽  
Trisomy 13

De novo translocation t(5;9)(q11.2;p22) associated with hydrops fetalis and cystic hygroma

2012 ◽  
Vol 31 (2) ◽  
pp. 39-42 ◽  
Author(s):  
Kristen Eisbrenner ◽  
Thora S. Steffensen ◽  
Valerie E. Whiteman ◽  
Enid Gilbert-Barness
Keyword(s):  
De Novo ◽  
Cystic Hygroma ◽  
Hydrops Fetalis ◽  
De Novo Translocation

scholarly journals Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: update on genetic testing in the NGS era

2019 ◽  
Vol 56 (10) ◽  
pp. 654-661 ◽  
Author(s):  
Kyra E Stuurman ◽  
Marieke Joosten ◽  
Ineke van der Burgt ◽  
Mariet Elting ◽  
Helger G Yntema ◽  
...  
Keyword(s):  
Pleural Effusion ◽  
Clinical Information ◽  
Nuchal Translucency ◽  
Cystic Hygroma ◽  
Hydrops Fetalis ◽  
Common Finding ◽  
Variable Degree ◽  
Renal Anomalies ◽  
Cardiac Defects ◽  
Ultrasound Findings

BackgroundThis study evaluates 6 years of prenatal rasopathy testing in the Netherlands, updates on previous data and gives recommendations for prenatal rasopathy testing.Methods424 fetal samples, sent in for prenatal rasopathy testing in 2011–2016, were collected. Cohort 1 included 231 samples that were sequenced for 1–5 rasopathy genes. Cohort 2 included 193 samples that were analysed with a 14-gene next generation sequencing (NGS) panel. For all mutation-positive samples in both cohorts, the referring physician provided detailed ultrasound findings and postnatal follow-up. For 168 mutation-negative samples in cohort 2, solely clinical information on the requisition form was collected.ResultsIn total, 40 (likely) pathogenic variants were detected (9.4%). All fetuses showed a variable degree of involvement of prenatal findings: increased nuchal translucency (NT)/cystic hygroma, distended jugular lymph sacs (JLS), hydrops fetalis, polyhydramnios, pleural effusion, ascites, cardiac defects and renal anomalies. An increased NT was the most common finding. Eight fetuses showed solely an increased NT/cystic hygroma, which were all larger than 5.5 mm. Ascites and renal anomalies appeared to be poor predictors of pathogenic outcome.ConclusionFetuses with a rasopathy show in general multiple ultrasound findings. The larger the NT and the longer it persists, the more likely it is to find a pathogenic variant. Rasopathy testing is recommended when the fetus shows an isolated increased NT ≥5.0 mm or when NT of ≥3.5 mm and at least one of the following ultrasound anomalies is present: distended JLS, hydrops fetalis, polyhydramnios, pleural effusion, ascites, cardiac defects and renal anomalies.

Cystic hygroma and hydrops fetalis in dup(11p) syndrome

1985 ◽  
Vol 22 (2) ◽  
pp. 287-289 ◽  
Author(s):  
J. P. Fryns ◽  
A. Kleczkowska ◽  
K. Vandenberghe ◽  
F. Moerman ◽  
H. Van den Berghe ◽  
...  
Keyword(s):  
Cystic Hygroma ◽  
Hydrops Fetalis

scholarly journals Hydrops fetalis with cystic hygroma: A case report

2012 ◽  
Vol 17 (2) ◽  
pp. 134-135 ◽  
Author(s):  
Mohammed Khairy Ali ◽  
Ahmed Y. Abdelbadee ◽  
Sherif A. Shazly ◽  
Essam R. Othman
Keyword(s):  
Case Report ◽  
Cystic Hygroma ◽  
Hydrops Fetalis
Sign in / Sign up

Export Citation Format

Share Document