Neuropediatrics 2007; 38(2): 64-70
DOI: 10.1055/s-2007-985137
Original Article

© Georg Thieme Verlag KG Stuttgart · New York

Ataxia, Delayed Dentition and Hypomyelination: A Novel Leukoencephalopathy

N. I. Wolf 1 , 2 , I. Harting 3 , A. M. Innes 4 , S. Patzer 5 , P. Zeitler 6 , A. Schneider 7 , A. Wolff 8 , K. Baier 9 , 10 , J. Zschocke 11 , F. Ebinger 1 , E. Boltshauser 2 , D. Rating 1
  • 1Department of Paediatric Neurology, University Children's Hospital, Heidelberg, Germany
  • 2Department of Neuropaediatrics, University Children's Hospital, Zurich, Switzerland
  • 3Department of Neuroradiology, University Hospital, Heidelberg, Germany
  • 4Department of Medical Genetics, Alberta Children's Hospital and University of Calgary, Calgary, Canada
  • 5Children's Hospital, Hospital St. Elisabeth und St. Barbara, Halle/Saale, Germany
  • 6Sozialpädiatrisches Zentrum, University Children's Hospital, Würzburg, Germany
  • 7Department of Paediatrics, Heidenheim, Hospital Heidenheim, Germany
  • 8Departments of Conservative Dentistry, University Hospital, Heidelberg, Germany
  • 9Department of Paediatric Dentistry, Alberta Children's Hospital, Calgary, Canada
  • 10Paediatric Dentistry, Cambridge and Kitchener, Canada
  • 11Institute of Human Genetics, University Hospital Heidelberg, Germany
Further Information

Publication History

received 11.10.2006

accepted 20.6.2007

Publication Date:
22 August 2007 (online)

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Abstract

We present four children, three of them boys, affected with an identical clinical pattern consisting of early-onset ataxia, delayed dentition, hypomyelination and cerebellar atrophy. Dental radiographs showed variable absence of succedaneous teeth. Proton MR spectroscopy in one child showed elevated white matter myo-inositol. As the clinical and radiological picture in these patients is identical to that of four cases described earlier, we suggest that this disorder with ataxia, delayed dentition and hypomyelination (ADDH) represents a new entity. With the characteristic tooth abnormalities it should be straightforward to identify new patients in order to facilitate the search for the underlying genetic defect.

References

Correspondence

Dr. N. I. Wolf

Department of Neuropaediatrics

University Children's Hospital

Im Neuenheimer Feld 150

69120 Heidelberg

Germany

Phone: +49/6221/5639321

Fax: +49/6221/565744

Email: nicole.wolf@med.uni-heidelberg.de