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Fırat Üniversitesi Sağlık Bilimleri Tıp Dergisi |
2000, Cilt 14, Sayı 2, Sayfa(lar) 355-358 |
[ Turkish ] [ PDF ] |
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 ] [ PDF ] |
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