Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature
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Anorectal malformations (ARM) range from mild anal to severe anorectal anomalies. Approximately 50% are estimated to be non-syndromic with multiple familial cases reported that suggest underlying genetic factors. These, however, still await identification.
Materials and methods
We report a familial case of non-syndromic ARM with a mother and her two children being affected. Mother and daughter had mild ARM that had only been diagnosed after the index patient was born with a more severe form and ultrashort Hirschsprung’s disease. To reveal the genetic cause in our family genome-wide array analysis was carried out to ascertain microaberrations characterized by loss or gain of genomic material. In addition, sequence analysis of four major Hirschsprung’s disease genes (RET, EDNRB, EDN3, and GDNF) and the HLXB9 gene was performed to identify a mutation common to all three family members; however, these analyses did not reveal any causal genetic alteration. To demonstrate the frequency of familial non-syndromic cases, we performed a literature search revealing 59 families with at least two affected members. Sufficient description of ARM phenotype and affection status of relatives to surely classify them as familial non-syndromic forms was given for 22 families.
The present family suggests that mild ARM may be overlooked in patients with non-specific clinical symptoms and that the incidence of ARM may thus be higher than previously estimated. With the new possibilities of whole exome sequencing, even small families hold the possibility to identify causal defects.
KeywordsAnal atresia Anorectal malformations Ultrashort Hirschsprung’s disease Multiplex family
We thank the family for their cooperation and continued interest in this research. We also thank the German self-help organization for patients with anorectal malformations (SoMA e.V.). We thank Pia Uerdingen for her excellent technical assistance and Dr. Christine Schmael for her expert advice on the manuscript. C. S., M. D., E. B., E. S., S. G., S. H., S. H.-C., M. M. N., M. L., and H. R. are members of the “Network for the Systematic Investigation of the Molecular Causes, Clinical Implications, and Psychosocial Outcome of Congenital Uro-Rectal Malformations (CURE-Net)” which is supported by a research grant (01GM08107) from the German Federal Ministry of Education and Research (Bundesministerium für Bildung und Forschung, BMBF). C.S. is supported by the BONFOR program of the University of Bonn, grant number O-149.0093.
- 8.Cozzi F, Wilkinson AW (1968) Familial incidence of congenital anorectal anomalies. Surgery 64:669–671Google Scholar
- 15.Gianferrari L, Cresseri A (1949) Su l’erediarietà dell’atresia anale. R C Classe di Sci 81:1Google Scholar
- 16.Hadra R (1885) Demonstration zweier Fälle von Atresia ani vulvalis. Berl Klin Wochenschr 21:340Google Scholar
- 23.Lojda Z, Gossrau R, Schiebler T (1979) Enzyme histochemistry: a laboratory manual. Springer, BerlinGoogle Scholar
- 27.Moore TC, Lawrence EA (1952) Congenital malformations of the rectum and anus; I. Clinical features and surgical management in 120 cases. Surgery 33:352–366Google Scholar
- 29.Murken JD, Devens K, Eversmann HJ (1969) Zur kausalen Genese der angeborenen Atresien des Verdauungstraktes. Z Kinderchir 7:326–333Google Scholar
- 34.Santulli TV (1962) In: Benson CD, Mustard WT, Ravitch MM, Snyder WH Jr, Welch KJ (eds) Pediatric surgery. Yearbook Publishers, Chicago, p 821Google Scholar
- 42.Van Gelder DW, Kloepfer HW (1961) Familial anorectal anomalies. Pediatrics 27:334–336Google Scholar