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Text
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URL Address
<a href="http://doi.org/10.1080/14767058.2017.1358263" target="_blank" rel="noreferrer noopener">http://doi.org/10.1080/14767058.2017.1358263</a>
Pages
2923–2929
Issue
21
Volume
31
Dublin Core
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Title
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Neonatal renal cystic diseases.
Publisher
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The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
Date
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2018
2018-11
Subject
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*Polycystic Kidney; Autosomal Dominant; Autosomal dominant polycystic kidney disease; Autosomal Recessive; autosomal recessive polycystic kidney disease; Humans; Impact of Events Scale; Infant; multicystic dysplastic kidney; neonatal renal cystic diseases; Newborn; Polycystic Kidney
Creator
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Khare Anshika; Krishnappa Vinod; Kumar Deepak; Raina Rupesh
Description
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PURPOSE: Neonatal renal cystic diseases have a great impact on the morbidity and mortality of the affected neonates and infants. A good insight into the pathophysiology, diagnosis and treatment options of various neonatal renal cystic diseases aid in early diagnosis and intervention, thereby preventing complications. METHODS: PubMed search was done for articles on "neonatal renal cystic diseases" and relevant publications including reviews were considered for our article. RESULTS: Both hereditary and nonhereditary causes of cystic kidney diseases can result in severe morbidity and mortality. The main diagnostic modality is ultrasound imaging and most of the neonatal renal cystic diseases are detected during prenatal ultrasound screening. Commonly encountered neonatal renal cystic diseases are autosomal dominant polycystic kidney disease, autosomal recessive polycystic kidney disease and multicystic dysplastic kidney. CONCLUSIONS: A thorough knowledge of various renal cystic diseases can be of extreme prognostic value. Physicians should be aware of the impact of early diagnosis and intervention on the lives of those affected. Further research about treatment of these diseases is ongoing and can result in breakthrough therapies for these patients.
Identifier
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<a href="http://doi.org/10.1080/14767058.2017.1358263" target="_blank" rel="noreferrer noopener">10.1080/14767058.2017.1358263</a>
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Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).
*Polycystic Kidney
2018
Autosomal Dominant
Autosomal dominant polycystic kidney disease
Autosomal Recessive
autosomal recessive polycystic kidney disease
Department of Internal Medicine
Humans
Impact of Events Scale
Infant
Khare Anshika
Krishnappa Vinod
Kumar Deepak
multicystic dysplastic kidney
NEOMED College of Graduate Studies Student
NEOMED College of Medicine
neonatal renal cystic diseases
Newborn
Polycystic Kidney
Raina Rupesh
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians