40 timestamped statements
across 3 collections
— auto-found in recorded discussions, each timestamp jumps to the exact moment.
Featured diaries
▶Ep 18 · 17:40
Cloacal exstrophy typically presents with persistent absent bladder visualization, normal amniotic fluid, low omphalocele, skin-covered spinal defects, and sometimes a prolapsed terminal ileum (elephant trunk sign) protruding through the abdominal wall defect.
Cloacal exstrophy typically presents with persistent absent bladder visualization, normal amniotic fluid, low omphalocele, skin-covered spinal defects, and sometimes a prolapsed terminal ileum (elephant trunk sign) protruding through the abdominal wall defect.
Cloacal exstrophy typically presents with persistent absent bladder visualization, normal amniotic fluid, low omphalocele, skin-covered spinal defects, and sometimes a prolapsed terminal ileum (elephant trunk sign) protruding through the abdominal wall defect.
Cloacal exstrophy typically presents with persistent absent bladder visualization, normal amniotic fluid, low omphalocele, skin-covered spinal defects, and sometimes a prolapsed terminal ileum (elephant trunk sign) protruding through the abdominal wall defect.
On ultrasound, the bladder is the first cystic structure seen from the abdominal cord insertion, outlined by umbilical arteries; a cystic structure posterior/inferior to the bladder reaching into the abdomen is hydrocolpos in a cloacal malformation.
On ultrasound, the bladder is the first cystic structure seen from the abdominal cord insertion, outlined by umbilical arteries; a cystic structure posterior/inferior to the bladder reaching into the abdomen is hydrocolpos in a cloacal malformation.
Prenatal Imaging and Counseling: Cloaca and Complex ARMs 2015
▶Ep 18 · 8:10
clinicalOn ultrasound, the bladder is the first cystic structure seen from the abdominal cord insertion, outlined by umbilical arteries; a cystic structure posterior/inferior to the bladder reaching into the abdomen is hydrocolpos in a cloacal malformation.↗
▶Ep 18 · 9:11
clinicalEchogenic concretions (meconium) in the hydrocolpos or bladder are clues for a recto-urinary fistula and anorectal malformation.↗
▶Ep 18 · 10:50
clinicalFetal MRI shows meconium as dark on T2-weighted imaging and bright on T1-weighted imaging; fluid in the fetal bowel is bright on T2 and dark on T1.↗
▶Ep 18 · 11:49
clinicalMeconium reaches the rectum by 20 weeks gestation and fills the entire colon by 26 weeks.↗
▶Ep 18 · 12:10
host_summaryOn fetal MRI sagittal view, the normal rectum measures at least 10 mm from the bladder base to its most distal segment (per Seinda et al.).↗
▶Ep 18 · 13:28
clinicalLong-common-channel cloaca on fetal MRI presents with a high-positioned, dilated rectum that funnels distally but does not reach far enough, and a thick-walled bladder due to outlet obstruction.↗
▶Ep 18 · 14:28
clinicalImperforate anus with recto-urinary fistula can show fluid distention of the rectum and enterocolitis on fetal MRI; increased fluid content (bright T2 signal instead of dark meconium) in a dilated rectum is a clue for recto-urinary fistula.↗
▶Ep 18 · 16:15
clinicalUrogenital sinus on fetal MRI shows a rectum following a normal posterior course (not dilated, reaching far enough), with hydrocolpos located between the bladder and rectum; this distinguishes it from short-common-channel cloaca.↗
▶Ep 18 · 17:40
clinicalCloacal exstrophy typically presents with persistent absent bladder visualization, normal amniotic fluid, low omphalocele, skin-covered spinal defects, and sometimes a prolapsed terminal ileum (elephant trunk sign) protruding through the abdominal wall defect.↗
▶Ep 18 · 20:20
clinicalCloacal exstrophy on fetal MRI shows no meconium signal in the expected distribution of the rectum, distinguishing it from bladder exstrophy (which has a normal rectum with dark T2/bright T1 meconium signal).↗
Prenatal Imaging and Counseling: Cloaca and Complex ARMs 2015
▶Ep 6 · 8:10
clinicalOn ultrasound, the bladder is the first cystic structure seen from the abdominal cord insertion, outlined by umbilical arteries; a cystic structure posterior/inferior to the bladder reaching into the abdomen is hydrocolpos in a cloacal malformation.↗
▶Ep 6 · 9:11
clinicalEchogenic concretions (meconium) in the hydrocolpos or bladder are clues for a recto-urinary fistula and anorectal malformation.↗
▶Ep 6 · 10:50
clinicalFetal MRI shows meconium as dark on T2-weighted imaging and bright on T1-weighted imaging; fluid in the fetal bowel is bright on T2 and dark on T1.↗
▶Ep 6 · 11:49
clinicalMeconium reaches the rectum by 20 weeks gestation and fills the entire colon by 26 weeks.↗
▶Ep 6 · 12:10
host_summaryOn fetal MRI sagittal view, the normal rectum measures at least 10 mm from the bladder base to its most distal segment (per Seinda et al.).↗
▶Ep 6 · 13:28
clinicalLong-common-channel cloaca on fetal MRI presents with a high-positioned, dilated rectum that funnels distally but does not reach far enough, and a thick-walled bladder due to outlet obstruction.↗
▶Ep 6 · 14:28
clinicalImperforate anus with recto-urinary fistula can show fluid distention of the rectum and enterocolitis on fetal MRI; increased fluid content (bright T2 signal instead of dark meconium) in a dilated rectum is a clue for recto-urinary fistula.↗
▶Ep 6 · 16:15
clinicalUrogenital sinus on fetal MRI shows a rectum following a normal posterior course (not dilated, reaching far enough), with hydrocolpos located between the bladder and rectum; this distinguishes it from short-common-channel cloaca.↗
▶Ep 6 · 17:40
clinicalCloacal exstrophy typically presents with persistent absent bladder visualization, normal amniotic fluid, low omphalocele, skin-covered spinal defects, and sometimes a prolapsed terminal ileum (elephant trunk sign) protruding through the abdominal wall defect.↗
▶Ep 6 · 20:20
clinicalCloacal exstrophy on fetal MRI shows no meconium signal in the expected distribution of the rectum, distinguishing it from bladder exstrophy (which has a normal rectum with dark T2/bright T1 meconium signal).↗
Prenatal Imaging and Counseling: Cloaca and Complex ARMs 2015
▶Ep 38 · 8:10
clinicalOn ultrasound, the bladder is the first cystic structure seen from the abdominal cord insertion, outlined by umbilical arteries; a cystic structure posterior/inferior to the bladder reaching into the abdomen is hydrocolpos in a cloacal malformation.↗
▶Ep 38 · 8:10
clinicalOn ultrasound, the bladder is the first cystic structure seen from the abdominal cord insertion, outlined by umbilical arteries; a cystic structure posterior/inferior to the bladder reaching into the abdomen is hydrocolpos in a cloacal malformation.↗
▶Ep 38 · 9:11
clinicalEchogenic concretions (meconium) in the hydrocolpos or bladder are clues for a recto-urinary fistula and anorectal malformation.↗
▶Ep 38 · 9:11
clinicalEchogenic concretions (meconium) in the hydrocolpos or bladder are clues for a recto-urinary fistula and anorectal malformation.↗
▶Ep 38 · 10:50
clinicalFetal MRI shows meconium as dark on T2-weighted imaging and bright on T1-weighted imaging; fluid in the fetal bowel is bright on T2 and dark on T1.↗
▶Ep 38 · 10:50
clinicalFetal MRI shows meconium as dark on T2-weighted imaging and bright on T1-weighted imaging; fluid in the fetal bowel is bright on T2 and dark on T1.↗
▶Ep 38 · 11:49
clinicalMeconium reaches the rectum by 20 weeks gestation and fills the entire colon by 26 weeks.↗
▶Ep 38 · 11:49
clinicalMeconium reaches the rectum by 20 weeks gestation and fills the entire colon by 26 weeks.↗
▶Ep 38 · 12:10
host_summaryOn fetal MRI sagittal view, the normal rectum measures at least 10 mm from the bladder base to its most distal segment (per Seinda et al.).↗
▶Ep 38 · 12:10
clinicalOn fetal MRI sagittal view, the normal rectum measures at least 10 mm from the bladder base to its most distal segment (per Seinda et al.).↗
▶Ep 38 · 13:28
clinicalLong-common-channel cloaca on fetal MRI presents with a high-positioned, dilated rectum that funnels distally but does not reach far enough, and a thick-walled bladder due to outlet obstruction.↗
▶Ep 38 · 13:28
clinicalLong-common-channel cloaca on fetal MRI presents with a high-positioned, dilated rectum that funnels distally but does not reach far enough, and a thick-walled bladder due to outlet obstruction.↗
▶Ep 38 · 14:28
clinicalImperforate anus with recto-urinary fistula can show fluid distention of the rectum and enterocolitis on fetal MRI; increased fluid content (bright T2 signal instead of dark meconium) in a dilated rectum is a clue for recto-urinary fistula.↗
▶Ep 38 · 14:28
clinicalImperforate anus with recto-urinary fistula can show fluid distention of the rectum and enterocolitis on fetal MRI; increased fluid content (bright T2 signal instead of dark meconium) in a dilated rectum is a clue for recto-urinary fistula.↗
▶Ep 38 · 16:15
clinicalUrogenital sinus on fetal MRI shows a rectum following a normal posterior course (not dilated, reaching far enough), with hydrocolpos located between the bladder and rectum; this distinguishes it from short-common-channel cloaca.↗
▶Ep 38 · 16:15
clinicalUrogenital sinus on fetal MRI shows a rectum following a normal posterior course (not dilated, reaching far enough), with hydrocolpos located between the bladder and rectum; this distinguishes it from short-common-channel cloaca.↗
▶Ep 38 · 17:40
clinicalCloacal exstrophy typically presents with persistent absent bladder visualization, normal amniotic fluid, low omphalocele, skin-covered spinal defects, and sometimes a prolapsed terminal ileum (elephant trunk sign) protruding through the abdominal wall defect.↗
▶Ep 38 · 17:40
clinicalCloacal exstrophy typically presents with persistent absent bladder visualization, normal amniotic fluid, low omphalocele, skin-covered spinal defects, and sometimes a prolapsed terminal ileum (elephant trunk sign) protruding through the abdominal wall defect.↗
▶Ep 38 · 20:20
clinicalCloacal exstrophy on fetal MRI shows no meconium signal in the expected distribution of the rectum, distinguishing it from bladder exstrophy (which has a normal rectum with dark T2/bright T1 meconium signal).↗
▶Ep 38 · 20:20
clinicalCloacal exstrophy on fetal MRI shows no meconium signal in the expected distribution of the rectum, distinguishing it from bladder exstrophy (which has a normal rectum with dark T2/bright T1 meconium signal).↗