ANORECTAL ATRESIA

 - IMPERFORATE ANUS

 

Anorectal malformations occur in 1:5000 live births and range in severity from a persistent cloaca to anal atresia (1,2). The anal canal is either absent or ends ectopically in a fistulous canal.
 

ETIOLOGY

 

Link to Etiology

 

 

CLASSIFICATION

 

 

ULTRASOUND

 

 

 

 

 

ASSOCIATED ANOMALIES (ABOUT 50%)

 

REFERENCES

  1. Boles ET Jr. Imperforate anus. Clin Perinatol 1978;5:149-161.
  2. Harris RD, Nyberg DA, Mack LA et.al. Anorectal atresia: Prenatal sonographic diagnosis. AJR 1987;145:395-400.
  3. Petrikovsky BM, Walzack MP, D'Addario PF. Fetal cloacal abnormalities; Prenatal sonographic findings and differential diagnosis. Obstet Gynecol 1988;72:464.
  4. Lande IM, Hamilton EF. The antenatal sonographic visualization of cloacal dysgenesis. J Ultrasound Med 1986;5:275.
  5. Bean WJ, Calonje MA, Aprill CN et.al. Anal atresia: A prenatal ultrasound diagnosis. J Clin Ultrasound 1978;6:73.
  6. Karrer FM, Flannery AM, Nelson MD et.al. Anorectal malformations: Evaluation of associated spinal dysraphic syndromes. J Pediatr Surg 1988;23:47.
  7. deVries PA, Cox KL. Surgery of anorectal anomalies. Surg Clin N Am 1985;65:1139.