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Persistent Cloaca

0 The most complex ARM in girls is when the rectum, vagina, and the last parts of the urinary system are combined into a single cavity.

0 Diagnosis is made clinically. If the external genital organs are small in girls with anal atresia, it should be considered.

0 Hydrocolpos is present in 50% of cases.

0 There is bilateral megaureter.

0 Associated with vaginal and uterine duplications or septations.

0 50% ARM is accompanied by additional anomaly. The frequency of additional anomaly in high and intermediate type is 2 times higher.

0 The most striking additional anomalies are vertebral (sacral) and urinary system anomalies.

0 Tethered cord is the most common example of spinal dysraphism with ARM.

0 The most common additional anomaly is the GENITOURIRINE SYSTEM anomalies. The most common GUS anomaly is vesicoureteral reflux (VUR). Renal agenesis and dysplasia are the second most common.

0 CVS anomalies; VSD, tetralogy of Fallot

0 GIS anomalies; Esophageal atresia is the most common.

0 is part of the VATER and VACTERL syndromes.

0 They are the most common malformations accompanying genitourinary system anomalies.

0 Perineal examination is very important.

0 In every newborn, even if the anus appears normal, it should be checked with a soft probe or with a finger.

0 Infants have bloating and fecaloid vomiting.

0 Chest X-ray, ECG, ECO, vertebral X-rays, SDAR are used in the diagnosis.

0 Pearl sign; In the scrotal raphe is white meconium.

0 Luggage handle sign; It is a skin fold where the anus should be.

0 When the baby cries, there is bulging where the anus should be.

0 Boys do not have folds between the glutes; flat hip sign

0 In order to detect the presence of a recto-urinary fistula, urine analysis must be performed.

0 After 24 hours after birth, the level of the anomaly is determined by invertogram.

0 The treatment is surgical and various procedures are applied according to the location and type of the anomaly.

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