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European Journal of Pediatrics

, Volume 170, Issue 6, pp 741–746 | Cite as

Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature

  • Charlotte Schramm
  • Markus Draaken
  • Gabriel Tewes
  • Enrika Bartels
  • Eberhard Schmiedeke
  • Stefanie Märzheuser
  • Sabine Grasshoff-Derr
  • Stuart Hosie
  • Stefan Holland-Cunz
  • Lutz Priebe
  • Martina Kreiß-Nachtsheim
  • Per Hoffmann
  • Stefan Aretz
  • Markus M. Nöthen
  • Heiko Reutter
  • Michael Ludwig
Original Paper

Abstract

Introduction

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.

Conclusion

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.

Keywords

Anal atresia Anorectal malformations Ultrashort Hirschsprung’s disease Multiplex family 

Notes

Acknowledgments

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.

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Copyright information

© Springer-Verlag 2010

Authors and Affiliations

  • Charlotte Schramm
    • 1
  • Markus Draaken
    • 1
    • 2
  • Gabriel Tewes
    • 3
  • Enrika Bartels
    • 1
  • Eberhard Schmiedeke
    • 4
  • Stefanie Märzheuser
    • 5
  • Sabine Grasshoff-Derr
    • 6
  • Stuart Hosie
    • 7
  • Stefan Holland-Cunz
    • 8
  • Lutz Priebe
    • 1
    • 2
  • Martina Kreiß-Nachtsheim
    • 1
  • Per Hoffmann
    • 1
    • 2
  • Stefan Aretz
    • 1
  • Markus M. Nöthen
    • 1
    • 2
  • Heiko Reutter
    • 1
    • 10
  • Michael Ludwig
    • 9
  1. 1.Institute of Human GeneticsUniversity of BonnBonnGermany
  2. 2.Department of Genomics, Life and Brain CenterUniversity of BonnBonnGermany
  3. 3.Department of Pediatric SurgeryEVK HammHammGermany
  4. 4.Department of Pediatric Surgery and UrologyCenter for Child and Adolescent Health, Hospital Bremen-MitteBremenGermany
  5. 5.Department of Pediatric SurgeryUniversity Hospital WürzburgWürzburgGermany
  6. 6.Department of Pediatric Surgery, Campus Virchow ClinicCharité University Hospital BerlinBerlinGermany
  7. 7.Department of Pediatric Surgery, Klinikum SchwabingTechnische Universität MünchenMunichGermany
  8. 8.Department of Pediatric SurgeryUniversity of HeidelbergHeidelbergGermany
  9. 9.Department of Clinical Chemistry and Clinical PharmacologyUniversity of BonnBonnGermany
  10. 10.Department of Neonatology, Children’s HospitalUniversity of BonnBonnGermany

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