Emanuel Sendromu

Kazandı M; Turan V; Zeybek B; Rgon A

EN TR

Emanuel Syndrome

Abstract

A 35 year old pregnant woman who had previous had a child by cesarean section and a previous abortion, was referred to our clinic because of an increased risk in a second trimester screening at 20 weeks. When we investigated with detailed ultrasonograpy, increased nuchal fold thickness, diaphragma hernia, complete endocardial cushion defect and truncus arteriosus were found. Amniosentesis was performed and the pregnancy was terminated medically with usage of vaginal and oral misoprostol. After chromosomal analysis, 47,.., +der(22) t(11,22) (q25;q13) was assigned. Although paternal chromosomes analysis was normal; maternal chromosomes corresponded with 46,XX t(11,22) (q25;q13), which is a carrier for this syndrome.

Keywords

Emanuel Syndrome, congenital malformations

Ayrıntılar

Birincil Dil

Türkçe

Konular

-

Bölüm

-

Yazarlar

Kazandı M

Turan V

Zeybek B

Rgon A

Yayımlanma Tarihi

1 Eylül 2010

Gönderilme Tarihi

1 Eylül 2010

Kabul Tarihi

-

Yayımlandığı Sayı

Yıl 1970 Cilt: 49 Sayı: 3

IZ

https://izlik.org/JA55SN58UN

Kaynak Göster

RIS / Bibtex

Vancouver

1.Kazandı M, Turan V, Zeybek B, Rgon A. Emanuel Sendromu. ETD [Internet]. 01 Eylül 2010;49(3):209-11. Erişim adresi: https://izlik.org/JA55SN58UN

Emanuel Sendromu

Emanuel Syndrome

Abstract

Keywords