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Dergiler / Turkish Journal of Medical Sciences / 2021 / Cilt: 51 - Sayı: 2

Demographic and clinical characteristics of children with autosomal dominant polycystic kidney disease: a single center experience

Belde KASAP DEMİR
Demet ALAYGUT
Caner ALPARSLAN
Eren SOYALTIN
Fatma MUTLUBAŞ
Seçil ARSLANSOYU ÇAMLAR
Önder YAVAŞCAN
Merve ARYA
Afig BERDELİ
Sayfa
772–777
Yayın Tarihi
2022-11-06
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The demographic, clinical, and laboratory findings were evaluated retrospectively.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Background/aim: In children with autosomal dominant polycystic kidney disease (ADPKD), clinical manifestations range from severe neonatal presentation to renal cysts found by chance.
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Temel Bulgular & Veri:Materials and methods: We evaluated children diagnosed with ADPKD between January 2006 and January 2019.
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Sonuç & Katkı:The demographic, clinical, and laboratory findings were evaluated retrospectively.
🔬Tür:Araştırma Makalesi
📍Kapsam:2006 Verileri
⚙️Değişkenler:Alan Parametreleri

Abstract

Background/aim: In children with autosomal dominant polycystic kidney disease (ADPKD), clinical manifestations range from severe neonatal presentation to renal cysts found by chance. We aimed to evaluate demographic, clinical, laboratory findings, and genetic analysis of children with ADPKD. Materials and methods: We evaluated children diagnosed with ADPKD between January 2006 and January 2019. The diagnosis was established by family history, ultrasound findings, and/or genetic analysis. The demographic, clinical, and laboratory findings were evaluated retrospectively. Patients

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Bu Makaleye Atıf Yap

DEMİR, B. K., ALAYGUT, D., ALPARSLAN, C., SOYALTIN, E., MUTLUBAŞ, F., ÇAMLAR, S. A., YAVAŞCAN, Ö., ARYA, M., BERDELİ, A. (2022). Demographic and clinical characteristics of children with autosomal dominant polycystic kidney disease: a single center experience. Turkish Journal of Medical Sciences, Cilt: 51 - Sayı: 2, 772–777. https://ajindex.com/articles/609952

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Kaynakça (10)

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