نتایج جستجو برای: renal agenesis

تعداد نتایج: 247722  

Journal: :Fertility and Sterility 2021

The study of the possible genetic causes complex genital malformations is a subject great interest both to know its etiology and diagnosis for best reproductive advice in these patients. Recently, Chen et al. (1Chen N. Zhao S. Jolly A. Wang L. Pan H. Yuan J. al.Perturbations genes essential Müllerian duct Wölffian development Mayer-Rokitansky-Küster-Hauser syndrome.Am J Hum Genet. 2021; 108: 1-...

Journal: :APSP journal of case reports 2016
Dilip Kumar Pal Vipin Chandra Manju Banerjee

Unilateral renal agenesis with vesicoureteral reflux in the ipsilateral full length ureter is a rare phenomenon. Herein we report a case of 10-year old boy who presented with recurrent urinary tract infections. No renal tissue was identified on left side in various imaging studies. Micturating cystourethrogram (MCUG) showed left sided refluxing and blind ending ureter. Left ureterectomy was don...

Journal: :European urology 2007
Antonio Carbone Giovanni Palleschi Giulio Tomiselli Maurizio Inghilleri Rocco Rago Andrea Lenzi Antonio Luigi Pastore

Few cases of unilateral renal agenesis associated with ipsilateral seminal vesicle ectasia or cyst have been reported. Two cases of unilateral renal aplastic dysplasia and ipsilateral ectopic ureter opening in the ejaculatory ducts associated with infertility secondary to bilateral obstruction of the seminal via are reported. Clinical and physical assessment including transrectal ultrasound and...

Journal: :Journal of medical genetics 2011
Cécile Jeanpierre Guillaume Macé Mélanie Parisot Vincent Morinière Audrey Pawtowsky Marion Benabou Jelena Martinovic Jeanne Amiel Tania Attié-Bitach Anne-Lise Delezoide Philippe Loget Patricia Blanchet Dominique Gaillard Marie Gonzales Wassila Carpentier Patrick Nitschke Frédéric Tores Laurence Heidet Corinne Antignac Rémi Salomon

BACKGROUND The RET/GDNF signalling pathway plays a crucial role during development of the kidneys and the enteric nervous system. In humans, RET activating mutations cause multiple endocrine neoplasia, whereas inactivating mutations are responsible for Hirschsprung disease. RET mutations have also been reported in fetuses with renal agenesis, based on analysis of a small series of samples. OB...

Journal: :The International journal of developmental biology 1992
J R Wenz M P Peck M J Murphy

Although renal agenesis and dysgenesis are relatively common and significant birth defects, no animal model to date has been utilized to adequately study these developmental pathologies. Blockage of the migration of the mesonephric duct in Day 2 chick embryos results in unilateral renal agenesis (URA) on the operated side, thus providing a model of chronic renal insufficiency. Embryos with URA ...

Journal: :Journal of Diagnostic Medical Sonography 1992

Journal: :Journal of Emergency Medicine, Trauma and Acute Care 2012

Journal: :Postgraduate medical journal 1969
A R Adamson B Benster

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید