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Polihidramniyozun Nadir Görülen İki Nedeni: Konjenital İshal ve Bartter Sendromu
2015
Journal:  
İstanbul Kanuni Sultan Süleyman Tıp Dergisi
Author:  
Abstract:

Polihidramniyoz yüksek riskli gebelik belirtisidir. Polihidramniyozla birlikte, perinatal morbidite ve mortalite artmaktadır. Etiyolojide annede diyabet, ikizden ikize kanama, plasental koryoanjioma, fetal anomali gibi sık görülen nedenler yanı sıra özellikle erken başlangıçlı ciddi polihidramniyoz olgularında; fetal renal tübülopati ve konjenital diyare gibi amniyotik sıvıyı arttıran daha nadir ciddi hastalıklar da yer almaktadır. Bu makalede, annelerinde nedeni belirlenemeyen polihidramniyoz öyküsü olan ve fetal poliüri ve ishalle teşhis edilen; yenidoğan döneminde “Neonatal Bartter Sendromu” ve “Konjenital İshal” tanısı alan iki olgumuz polihidramniyozun nadir nedenleri olarak sunulmuştur.

Keywords:

Two rare causes of polihidramniosis: congenital ishal and Bartter syndrome
2015
Author:  
Abstract:

Polyhydramniosis is a high-risk pregnancy sign. With polyhydramniosis, perinatal morbidity and mortality increases. The etiology includes common causes such as diabetes in the mother, twin-to-twin bleeding, placental coryoanjioma, fetal anomaly, and especially in early serious polihidramniosis events; fetal renal tubulopathy and congenital diarrhea, more rare serious diseases that increase the amniotic fluid. In this article, two of our phenomena, with an uncoverable history of polihidramniosis in their mothers and diagnosed with fetal polyurethane and diarrhea; diagnosed with "Neonatal Bartter Syndrome" and "Congenital Ishal" in the newborn period, are presented as rare causes of polihidramniosis.

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İstanbul Kanuni Sultan Süleyman Tıp Dergisi

Field :   Sağlık Bilimleri

Journal Type :   Ulusal

Metrics
Article : 386
Cite : 360
2023 Impact : 0.026
İstanbul Kanuni Sultan Süleyman Tıp Dergisi