Abstract of imperforate anus

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In addition, imperforate anus is associated with atypical anal appearance 6 or, if it is associated with a fistula to the urinary system, the presence of intraluminal colonic calcifications 7 in the third trimester.

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Oct 01, · The omphalocele-exstrophy-imperforate anus-spinal defects complex is a severe multisystem congenital defect. To comprehensively care for these patients one must appreciate the neurological and orthopedic impact on the overall health of the child.


Abstract. OBJECTIVE: To provide a follow-up of patients with cloacal malformations seen by the author from to SUMMARY BACKGROUND DATA: Cloaca, which occurs in approximately 1 of 50, births, is the most complex type of imperforate anus with confluence of the rectum, vagina, and bladder in a urogenital sinus. Abstract. Imperforate anus or anorectal atresia is often associated with major fetal structural defects but it may also be an isolated abnormality. Prenatal diagnosis is difficult but may be assisted by ultrasound detection of enterolithiasis in dilated bowel and confirmed by MRI study.
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Imperforate anus is a rare inborn abnormality characterized by the absence or abnormal localization of the anus. The rectum or the colon may be connected to the vagina or the bladder by a tunnel (fistula). With surgical correction, normal elimination can become possible.

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Anal atresia, or imperforate anus, refers to a spectrum of anorectal abnormalities ranging from a membranous separation to complete absence of the anus. Epidemiology The estimated incidence is 1 . Imperforate anus is a common congenital anomaly necessitating extensive surgery in neonates. The low type of imperforate anus passes through the levator ani muscle group and through its central puborectalis muscle, the major determinant of fecal continence.

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Keywords: Anus, Imperforate anus, Ultrasound (US), Ultrasonography, Infant In terms of the diagnostic evaluation of neonates with an imperforate anus (IA), the primary goal is the differentiation of IA type, as this information is required to determine the correct type of surgery. Abstract. Imperforate hymen diagnosed beyond the newborn period may present a dilemma for the physician. Three case studies are reviewed in which children with the diagnoses of imperforate hymen presented for evaluation of suspected sexual abuse.

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An imperforate anus or anorectal malformations (ARMs) are birth defects in which the rectum is malformed. ARMs are a spectrum of different congenital anomalies in males and females which vary from fairly minor lesions to complex anomalies. Adult presentation of a rectocutaneous fistula with imperforate anus is rare. We report the case of a year-old man who presented with an anorectal malformation and a rectocutaneous fistula. The patient complained of faecal matter passing through the external orifis of a .
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Abstract Objective. Despite the relatively common occurrence of imperforate anus, prenatal diagnosis is rarely reported. In this study, we investigated the presence and diagnosis of imperforate anus along with strategies for improving prenatal diagnosis of the condition. Patients and methods.

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