Brief clinical report: not all cystic hygromas occur in the Ullrich-Turner syndrome.
Publication/Presentation Date
7-1-1982
Abstract
We report two sib fetuses with nuchal systic hygroma and cleft palate. This condition is probably recessively inherited as the parents have normal chromosomes (G-banded) and the fetuses were of opposite sex. Nuchal cystic hygroma is a nonspecific malformation, which reflects a delay in development of the connection between the jugular lymph sacs and the internal jugular vein. This fetal malformation and its equivalent in the adult, neck webbing, has been reported to be a part of a variety of genetic malformation syndromes. Some suggestions for counseling parents of an affected fetus are made: If the chromosome karyotype of an affected fetus is unknown, ultrasound examination, rather than AFP studies, is suggested for future pregnancies.
Volume
12
Issue
3
First Page
327
Last Page
331
ISSN
0148-7299
Published In/Presented At
Cowchock, F. S., Wapner, R. J., Kurtz, A., Chatzkel, S., Barnhart, J. S., Jr, & Lesnick, D. C. (1982). Brief clinical report: not all cystic hygromas occur in the Ullrich-Turner syndrome. American journal of medical genetics, 12(3), 327–331. https://doi.org/10.1002/ajmg.1320120310
Disciplines
Medicine and Health Sciences
PubMedID
7114094
Department(s)
Department of Obstetrics and Gynecology
Document Type
Article