[ Ana Sayfa | Editörler | Danışma Kurulu | Dergi Hakkında | İçindekiler | Arşiv | Yayın Arama | Yazarlara Bilgi | E-Posta ]
Fırat Üniversitesi Sağlık Bilimleri Tıp Dergisi
2000, Cilt 14, Sayı 2, Sayfa(lar) 355-358
[ Turkish ]
Infantil Polycytic Kindey Disease (Potter’s I). A Case Report
Hüsnü ÇELİK, Ekrem SAPMAZ, Dr. Ebru GÖZERİ, Leyla ÖZCEYHAN BEYTUR, Aygen ALTINGÜL
Fırat Üniversitesi Tıp Fakültesi, Elazığ-TÜRKİYE
Keywords: Infantile polycystic kidney, Prenatal diagnosis

Objective:İnfantil polycystic kindey is an autosomal recessive disorder that seen rare. Because of delayed prenatally diagnosed our case, the literature were rewieved.

Case: The case is that 37th week gestational age and two degree marriage family. She have been sent by doctor that done controls of antenatal period with diagnosed oligohydroamniosis and mass in abdomen.

Conclusion: Infantil polycystic kidney disease can diagnose on the prenatal period. It’s prognosis is bad. Most of the cases die at the early neonatal period. It’s early diagnose is important.


[ Turkish ]
[ Ana Sayfa | Editörler | Danışma Kurulu | Dergi Hakkında | İçindekiler | Arşiv | Yayın Arama | Yazarlara Bilgi | E-Posta ]