نتایج جستجو برای: fetal hydronephrosis

تعداد نتایج: 89906  

2016
Mee Kyung Namgoong

Nephrogenic diabetes insipidus (NDI) can cause nonobstructive hydronephrosis. Congenital NDI (CNDI) is caused by a genetic mutation. This case report presents a 12-year-old girl who was incidentally diagnosed with nonobstructive hydronephrosis due to NDI caused by AQP2 gene mutation after being evaluated for microscopic hematuria found on routine health examination at school. The patient’s medi...

Journal: :The Japanese Journal of Urology 1949

Journal: :The Japanese Journal of Urology 1982

Journal: :Kathmandu University medical journal 2016
R Shrestha R M Shakya A Khan A

Background Renal colic is a common emergency department presentation. Hydronephrosis is indirect sign of urinary obstruction which may be due to obstructing ureteric calculus and can be detected easily by bedside ultrasound with minimal training. Objective To compare the accuracy of detection of hydronephrosis performed by the emergency physician with that of radiologist's in suspected renal co...

2010
Kenneth J. Perry Paul Ko Peter Mariani A. James Ciaccio

A previously healthy 25-year-old man presented to a community emergency department (ED) with two hours of sharp, intermittent, right-sided flank pain associated with hematuria. Vital signs showed no fever or tachycardia. Abdominal and genitourinary exam were benign. The patient was given analgesia while blood and urine samples were collected. Non-contrast computed tomography (CT) was ordered to...

Journal: :Revista espanola de medicina nuclear e imagen molecular 2015
T K Jain R K Basher B R Mittal A Bhatia K L N Rao

Hydronephrosis is a common finding in urinary tract outflow obstruction. Chronically obstructed hydronephrotic system may be associated with parenchymal changes. Ultrasound, intravenous urography, micturating cysto-urethrogram and scintigraphy are commonly performed to evaluate the cause of obstruction. In childhood, pelviureteric junction obstruction is a common cause of the hydronephrosis. Hy...

Journal: :Revista do Hospital das Clinicas 2004
Lilian Maria José Albano Paula Priscila Ohara Sakae Marta Maria Galli Bozzo Mataloun Clea Rodrigues Leone Débora R Bertola Chong Ae Kim

Schinzel-Giedion syndrome is a rare autosomal recessive disorder characterized by coarse facies, midface retraction, hypertrichosis, multiple skeletal anomalies, and cardiac and renal malformations. Craniofacial abnormalities of this syndrome sometimes resemble a storage or metabolic disease. The pathogenesis of the disease remains unknown. The objective of this report was to emphasize the impo...

2006
Tae-Hyun Yoo Dong-Ryeol Ryu Young Soo Song Sang Chul Lee Hyung Jong Kim Joo Seong Kim Hoon Young Choi Shin-Wook Kang

Most cases of hydronephrosis are caused by urinary tract obstruction. However, excessive polyuric syndrome rarely gives rise to non-obstructive hydronephrosis, megaureter, and a distended bladder. The authors report here on two cases of congenital nephrogenic diabetes insipidus (NDI) with severe bilateral hydronephrosis and megaureter. It is Interesting that the patients were symptomless except...

Journal: :Developmental period medicine 2016
Grażyna Krzemień Agnieszka Szmigielska Przemysław Bombiński Marzena Barczuk Agnieszka Biejat Stanisław Warchoł Teresa Dudek-Warchoł

BACKGROUND Hydronephrosis is the one of the most common congenital abnormalities of urinary tract. The left kidney is more commonly affected than the right side and is more common in males. AIM OF THE STUDY To determine the role of ultrasonography, renal dynamic scintigraphy and lowerdose computed tomography urography in preoperative diagnostic workup of infant with extreme hydronephrosis. ...

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