SoMA is the German patient organization for people with an anorectal malformation (children born without an anus or with an anus ending in a wrong location) and Hirschsprung’s disease. Anorectal malformations may be associated with further malformations (e.g. bladder, sexual organs, spine, or cardiac defects) and the patients often face lifelong problems such as incontinence. Because of the lac...

Diphallia is a very rare congenital anomalies occurs 1: 5-6 Million live birth. Associated like imperforate anus, vertebral deformities, double bladder, exstrophy of the cloacae, and duplication recto sigmoid may in association with this. Amongst all anorectal malformations common anomaly that can occur diphallia. Here we are presenting neonate functional penis, partial scrotal dysraphism, high...

Aim: To assess the effectiveness of posterior sagittal anorectplasty for repair anorectal malformations in terms postoperative complications and functional outcomes. Study design: Descriptive prospective study. Place duration study: Sahiwal Teaching Hospital, Sahiwal. From 1st January 2016 to 31st December 2019. Methodology: Forty-two children with high/intermediate malformations, who underwent...

A 2-day-old male baby presented with abdominal distension and failure to pass meconium. The perineal examination revealed normally placed patent anus. A rectal examination with thermometer revealed a resistance at 2-3cm from the anal verge. A contrast enema was given to document the suspicion of rectal atresia. The contrast enema revealed a 2cm long stenosis of the rectum opening abruptly into ...

Pearls of meconium can be seen on the raphe of the scrotum and are considered as a sign of anorectal malformation (ARM). Scrotal pearls without ARM are rare in children and designated as median raphe cyst of the scrotum (MRC). A six-month-old boy with scrotal pearls without ARM is presented to discuss the clinical features and treatment modalities of MRC in infants.