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Journals / Pediatrik Cerrahi Derg. / 1995 / Cilt: 9 - Sayı: 2

Multicystic dysplastic kidney: Prenatal diagnosis and postnatal management

Haluk SARIHAN
Rahmi AKYAZICI
Musa ABEŞ
Şirin GÜLKÖK
Kemal SERÇE
Pages
356–358
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Prenatal diagnosis of MCDK has provided for a clear line of management and no complications have been encountered with this approach.

📌 3 Key Takeaways

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Objective & Hypothesis:Six infants with multicystic dysplastic kidneys (MCDK) diagnosed prenatally with ultrasonography.
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Key Findings & Data:Therefore five, patients were operated by the sixth month.
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Conclusion & Impact:Prenatal diagnosis of MCDK has provided for a clear line of management and no complications have been encountered with this approach.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Süt çocuğu · Süt çocuğu · yenidoğan

Abstract

Six infants with multicystic dysplastic kidneys (MCDK) diagnosed prenatally with ultrasonography. One female infant also had a large ovarian cyst. The kidneys were palpable in four newborns at first physical examination. During the first six months, it was established that minimal change occured in kidney morphology. Therefore five, patients were operated by the sixth month. One patient was lost to follow up. Prenatal diagnosis of MCDK has provided for a clear line of management and no complications have been encountered with this approach.

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Cite This Article

SARIHAN, H., AKYAZICI, R., ABEŞ, M., GÜLKÖK, Ş., SERÇE, K. (1995). Multicystic dysplastic kidney: Prenatal diagnosis and postnatal management. Pediatrik Cerrahi Derg., Cilt: 9 - Sayı: 2, 356–358. https://ajindex.com/articles/285495