Hydronephrosis congenital

Common Name(s)

Hydronephrosis congenital

Description for this condition is not yet available.
 

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Condition Specific Organizations

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Hydronephrosis congenital" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Hydronephrosis congenital" returned 25 free, full-text research articles on human participants. First 3 results:

ATP5B and ETFB metabolic markers in children with congenital hydronephrosis.
 

Author(s): Qi Zhao, Yi Yang, Changlin Wang, Ying Hou, Hui Chen

Journal: Mol Med Rep. 2016 Dec;14(6):5111-5115.

 

Congenital obstructive nephropathy is the primary cause of chronic renal failure in children. Disorders of mitochondrial energy metabolism may be a primary factor underlying tubular cell apoptosis in hydronephrosis. The β-F1-ATPase (ATP5B) and electron transfer flavoprotein β subunit ...

Last Updated: 14 Nov 2016

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Congenital Nephrogenic Diabetes Insipidus Presented With Bilateral Hydronephrosis and Urinary Infection: A Case Report.
 

Author(s): Kewen Zheng, Yi Xie, Hanzhong Li

Journal: Medicine (Baltimore). 2016 May;95(22):e3464.

 

Nephrogenic diabetes insipidus (NDI) is a condition resulting from the kidney's impaired response to circulating antidiuretic hormone (ADH), leading to polydipsia and polyuria. Urinary tract dilatation caused by NDI is a rare situation. Here, we report a case of congenital NDI presented ...

Last Updated: 4 Jun 2016

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Unilateral congenital giant megaureter with renal dysplasia compressing contralateral ureter and causing bilateral hydronephrosis: a case report and literature review.
 

Author(s): Mingming Yu, Geng Ma, Zheng Ge, Rugang Lu, Yongji Deng, Yunfei Guo

Journal:

 

Congenital giant megaureter (CGM) is uncommon in the pediatric population. The major clinical presentations are marked protruberances and abdominal cysts.

Last Updated: 10 Feb 2016

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Hydronephrosis congenital" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Ambulatory Blood Pressure Measurement in Children With Congenital Urine Flow Obstruction
 

Status: Available

Condition Summary: Hydronephrosis; Multicystic-Dysplastic Kidney

 

Last Updated: 1 Oct 2008

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CTT on Renogram as an Early Marker of Significant Obstruction in Uretero-pelvic Junction Syndrome
 

Status: Not yet recruiting

Condition Summary: Ureteropelvic Junction Obstruction

 

Last Updated: 17 Jan 2017

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Indwelling Double-J Ureteral Stent Versus Externalized Modified-Salle Stent for Pyeloplasty
 

Status: Recruiting

Condition Summary: Ureteropelvic Junction Obstruction

 

Last Updated: 13 Sep 2016

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