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Beverly G. Coleman, MD, FACR
The Fetal Genitourinary Tract
Beverly G. Coleman, MD, FACR
01/14/2013 | Time : 48 min
About This Lecture:

Topics mentioned in this video : Title, Normal fetal kidneys, Normal urinary tract, Normal fetal bladder, Normal urinary tract, Normal fetal adrenal glands, Fetal genitalia, Fetal urine production, Normal urinary tract, Systematic approach to the abnormal urinary tract, Renal developmental variants, Renal agenesis – unilateral/bilateral, Unilateral renal agenesis, Bilateral renal agenesis, BRA in VATERL, Renal ectopia, Pelvic kidney, Is one kidney truly missing?, No RUA & dysplastic right pelvic kidney, Horseshoe kidney, Horseshoe kidney at 17 weeks, Horseshoe kidney with dysplasia, Crossed renal ectopia, Crossed fused renal ectopia, “Pancake” kidney, Urinary tract obstruction, Mild renal pyelectasis, Unilateral mild pyelectasis or normal?, Extra renal pelvis in a pelvic kidney, Society of fetal urology grading, Criteria for significant hydronephrosis, Ureteropelvic junction obstruction, Bilateral mild UPJ obstruction, Unilateral UPJ 19 weeks, Blown out UPJ, Ureterovesicle pathology, Duplicated collecting system, Duplicated collecting system?, Ectopic ureters, Duplication – severe UP obstruction and LP reflux, Unilateral duplication reflux > obstruction, Bilateral duplications, Postnatal outcome, AP diameter, Congenital megaureter, Lower urinary tract obstruction, Posterior urethra “keyhole”, Bladder volume 80ml, Obstructive cystic dysplasia, LUTO at 21 weeks, Segmental dysplasia at 20 weeks, Value of sonographic criteria in the prediction of renal dysplasia, Hyperechoic kidneys, Normal size echogenic kidneys, IVF DC/DA 26 week twins, LUTO at 21 weeks, Massive urinary ascites, Fetal urinary biochemistry, Causes of distended bladder, GU anomalies, Megalourethra, MMIHS, Renal cystic disease, Multicystic dysplastic kidney, Unilateral MCDK, MCDK, Multicystic dysplastic kidney, Bilateral MCDK, Autosomal recessive polycystic kidney disease, ARPKD, Polycystic reanl disease, ARPKD 9 MHz, ARPKD 8MHz TV, ADPKD, Conclusions

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Keywords : /limb anomalies, ADPKD, AFI, AFV, amniotic fluid index, amniotic fluid volume, amniotic fluid, ARPKD, autosomal dominant polycystic kidney disease, Autosomal Recessive Polycystic Kidney Disease, color Doppler, congenital megaureter, corticomedullary differentiation, crossed fused renal ectopia, crossed renal ectopia, deepest vertical pocket, duplicated collecting system, DVP, dysplastic kidney, echogenic kidneys, ectopic ureters, extra renal pelvis, fetal adrenal glands, fetal bladder, fetal kidneys, fetal ultrasound, fetal ureters, horseshoe kidney, hydronephrosis, keyhole sign, lower urinary tract obstruction, LUTO, MCDK, megacystis-microcolon-intestinal hypoperistalsis syndrome, megalourethra, MMIHS, Multicystic dysplastic kidney, obstetrical ultrasound, obstruction cystic dysplasia, oligohydramnios, pancake kidney, pelvic kidney, posterior urethral valves, Potter syndrome, pyelocaliectasis, renal agenesis, renal artery, renal cortex, renal cyst, renal ectopia, renal isthmus, renal pelves, renal pelvis, renal pyelectasis, renal pyramids, renal vein, umbilical artery, UPJ obstruction, ureterocele, ureteropelvic junction obstruction, urinary ascites, urinoma, VATERL, vertebral defects/imperforate anus/tracheoesophageal fistula/radial and renal dysplasia

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