Gonca ÖZTEN, Mehmet Sinan BEKSAÇ, Canan ÜNAL, Erdem FADILOĞLU, Beril TALİM

Ullrich Konjenital Muskuler Distrofinin Prenatal Tanısı

Amaç: Bu çalışmada, önceki çocuğunda Ullrich konjenital müsküler distrofi tanısı olan hastaların, sonraki gebeliklerinde prenatal tanı amaçlı uygulanan koryon villus örneklemelerinin değerlendirilmesi amaçlandı.Gereç ve Yöntemler: 2011 ile 2017 yılları arasında, Hacettepe Üniversitesi Kadın Hastalıkları ve Doğum Kliniği, Perinatoloji Bilim Dalı’nda daha önceki çocuklarında Ullrich Konjenital Müsküler Distrofi mevcut olan beş gebenin prenatal tanı amaçlı yapılan koryon villus örneklemesi sonuçları geriye dönük olarak değerlendirildi ve gebelik sonuçları incelendi.Bulgular: Çalışmaya alınan 5 gebenin, biri ikiz gebelik olmak üzere toplam 9 fetusuna ait koryon villus örnekleri değerlendirildi. Altı fetus’da Kollajen VI pozitif olarak tespit edildi ve bu olgularda term doğum gerçekleştirildi. Üç sonuç ise Kollajen VI negatif olarak saptandı ve onamları alındıktan sonra aile kararı ile terminasyon uygulandı.Sonuç: Klinik olarak büyük öneme sahip olan Ullrich Konjenital Müsküler Distrofi gibi nadir konjenital muskuler distrofilerde indeks vaka varlığında yapılacak olan prenatal tanı çalışmaları iyi tıbbi uygulamalar açısından büyük öneme sahiptir.

Anahtar Kelimeler:

Ullrich konjenital musküler distrofi, prenatal tanı, kollajen VI

Prenatal Diagnosis Of Ullrich Congenital Muscular Dystrophy

Aim: In this study, we aimed to evaluate prenatal diagnosis of Ullrich Congenital Muscular Dystrophy at the pregnancies with a previous child with the disease.Material and Methods: The results of chorionic villus sampling for the prenatal diagnosis of Ullrich Congenital Muscular Dystrophy at five families with a previous child with the disease. Results of the prenatal diagnostic tests and pregnancy outcomes were evaluated. The study included patients got delivered between 2011 and 2017 at the Hacettepe University Obstetrics and Gynecology Clinic, Perinatology Department.Results: Chorionic villi samples of 9 fetuses, including 5 pregnant women including 8 pregnancies one twin pregnancy were evaluated. Collagen VI was detected as positive in six fetuses and all of these patients delivered at term. Three out of nine chorionic villus samples were found to be negative for Collagen VI and termination was performed after detailed consent of the families.Conclusions: Prenatal diagnostic studies for rare congenital muscular dystrophies such as Ullrich Congenital Muscular Dystrophy, which has a clinically large significance and morbidity, have great prospects for good medical practice.

Keywords:

Ullrich coıngenital muscular dystrophy, prenatal diagnosis, collagen VI,

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