지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2023.3
- 수록면
- 28 - 35 (8page)
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초록· 키워드
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The polycystic kidney disease (PKD) is a genetic disease that can be classified into 2 groups: autosomal dominant and autosomal recessive. Autosomal dominant PKD has a mild to moderate clinical course with an average onset after adulthood. Autosomal recessive PKD can have life-threatening manifestations during the neonatal period, even before birth. Daegu Catholic Universtiy Medical Center had a prenatally diagnosed case of a known autosomal dominant PKD and the fetus suffering fetal hydrops due to severely enlarged polycystic kidneys. A cesarean section was performed at 34 weeks of gestation due to severe fetal hydrops. To relieve abdominal compartment syndrome, the neonate underwent unilateral nephrectomy just after birth but expired 4 days later due to respiratory distress. Hence, there can be a rare but possible case of fatal neonatal outcome in a mother with autosomal dominant PKD. Therefore, we recommend close observation and multifaceted counseling for the patient with family history of autosomal dominant PKD.
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