Persistent cloaca is a very rare congenital anomaly with a single common perineal opening for the genital, urinary and gastrointestinal tracts, which arises from defects in the embryonal process of descent of urorectal septum or fusion to cloacal membrane. Anomalies associated with persistent cloaca are found in the upper urinary tract, gastrointestinal tract, cardiovascular system, central nervous system and respiratory system, which are not easily detected through ultrasound during pregnancy. It has been reported that if those anomalies are diagnosed early, they can be corrected surgically. We present a case of persistent cloaca with hydrocolpos confirmed by autopsy after emergency cesarean section which was initially presented as a huge ...
Persistent cloaco is the most severe type of anorectal malformation encountered in children. Patient...
INTRODUCTION: A cloaca occurs when genitourinary tract and bowel converge into a common channel. We ...
AbstractObjectiveTo present female pseudohermaphroditism in a prenatally diagnosed cloacal malformat...
A 40-year-old, primigravid woman presented at 23 weeks of gestation for evaluation of an extra-abdom...
[[abstract]]A 40-year-old, primigravid woman presented at 23 weeks of gestation for evaluation of an...
AbstractA 40-year-old, primigravid woman presented at 23 weeks of gestation for evaluation of an ext...
This is a case report of prenatal observation of uteravaginal duplication in a fetus with a complica...
AbstractA 40-year-old, primigravid woman presented at 23 weeks of gestation for evaluation of an ext...
SummaryObjectivePrenatal diagnosis of a cloacal anomaly is difficult. Magnetic resonance imaging (MR...
Introduction: Cloacal malformation is an extremely rare fetal pathological condition but an importan...
Cloacal exstrophy is a rare congenital disorder that may lead to mortality and morbidity. Although t...
Persistent cloaco is the most severe type of anorectal malformation encountered in children. Patient...
Abstract Background Urorectal septum malformation sequence (URSMS) is characterized by incomplete pa...
Cloacal exstrophy is a rare congenital disorder that may lead to mortality and morbidity. Although t...
Hydrometrocolpos, occurring in approximately 1/6000 newborn girls, can be caused by a stenotic uroge...
Persistent cloaco is the most severe type of anorectal malformation encountered in children. Patient...
INTRODUCTION: A cloaca occurs when genitourinary tract and bowel converge into a common channel. We ...
AbstractObjectiveTo present female pseudohermaphroditism in a prenatally diagnosed cloacal malformat...
A 40-year-old, primigravid woman presented at 23 weeks of gestation for evaluation of an extra-abdom...
[[abstract]]A 40-year-old, primigravid woman presented at 23 weeks of gestation for evaluation of an...
AbstractA 40-year-old, primigravid woman presented at 23 weeks of gestation for evaluation of an ext...
This is a case report of prenatal observation of uteravaginal duplication in a fetus with a complica...
AbstractA 40-year-old, primigravid woman presented at 23 weeks of gestation for evaluation of an ext...
SummaryObjectivePrenatal diagnosis of a cloacal anomaly is difficult. Magnetic resonance imaging (MR...
Introduction: Cloacal malformation is an extremely rare fetal pathological condition but an importan...
Cloacal exstrophy is a rare congenital disorder that may lead to mortality and morbidity. Although t...
Persistent cloaco is the most severe type of anorectal malformation encountered in children. Patient...
Abstract Background Urorectal septum malformation sequence (URSMS) is characterized by incomplete pa...
Cloacal exstrophy is a rare congenital disorder that may lead to mortality and morbidity. Although t...
Hydrometrocolpos, occurring in approximately 1/6000 newborn girls, can be caused by a stenotic uroge...
Persistent cloaco is the most severe type of anorectal malformation encountered in children. Patient...
INTRODUCTION: A cloaca occurs when genitourinary tract and bowel converge into a common channel. We ...
AbstractObjectiveTo present female pseudohermaphroditism in a prenatally diagnosed cloacal malformat...