| Literature DB >> 17712733 |
N I Wolf1, I Harting, A M Innes, S Patzer, P Zeitler, A Schneider, A Wolff, K Baier, J Zschocke, F Ebinger, E Boltshauser, D Rating.
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.Entities:
Mesh:
Year: 2007 PMID: 17712733 DOI: 10.1055/s-2007-985137
Source DB: PubMed Journal: Neuropediatrics ISSN: 0174-304X Impact factor: 1.947