Antenatal diagnosis of a rare fetal syndrome : is this a new syndrome or a variant of goldston syndrome ?

Author

al-Shahrani, Misfir S.

Source

Bahrain Medical Bulletin

Issue

Vol. 34, Issue 2 (30 Jun. 2012), pp.1-5, 5 p.

Publisher

King Hamad University Hospital

Publication Date

2012-06-30

Country of Publication

Bahrain

No. of Pages

5

Main Subjects

Medicine

Topics

Abstract EN

Goldston Syndrome is a rare condition characterized by polycystic enlarged kidneys and Dandy-Walker Malformation.

It is a rare variant of Meckel Gruber Syndrome.

A case with a possible diagnosis of Goldston syndrome is presented; the diagnosis was made by fetal ultrasound at 30 weeks of gestation in 25 years old Saudi mother who had previous pregnancies with congenital malformations.

Ultrasound of the fetus showed severe olighydramnios, Dandy-Walker malformation, enlarged echogenic kidneys and fetal ascites.

To my knowledge, this is the fifth case of Goldston syndrome diagnosed during intrauterine life or could be a new entity because of fetal ascites.

American Psychological Association (APA)

al-Shahrani, Misfir S.. 2012. Antenatal diagnosis of a rare fetal syndrome : is this a new syndrome or a variant of goldston syndrome ?. Bahrain Medical Bulletin،Vol. 34, no. 2, pp.1-5.
https://search.emarefa.net/detail/BIM-602699

Modern Language Association (MLA)

al-Shahrani, Misfir S.. Antenatal diagnosis of a rare fetal syndrome : is this a new syndrome or a variant of goldston syndrome ?. Bahrain Medical Bulletin Vol. 34, no. 2 (Jun. 2012), pp.1-5.
https://search.emarefa.net/detail/BIM-602699

American Medical Association (AMA)

al-Shahrani, Misfir S.. Antenatal diagnosis of a rare fetal syndrome : is this a new syndrome or a variant of goldston syndrome ?. Bahrain Medical Bulletin. 2012. Vol. 34, no. 2, pp.1-5.
https://search.emarefa.net/detail/BIM-602699

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references : p. 5

Record ID

BIM-602699