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Dentatorubropallidoluysian Atrophy in Chinese
I-Hui Lee, MD;
Bing-Wen Soong, MD, PhD;
Yi-Chun Lu, BS;
Yue-Cune Chang, PhD
Arch Neurol. 2001;58:1905-1908.
Background Dentatorubropallidoluysian atrophy (DRPLA) is a
rare, autosomal dominant neurodegenerative disease characterized by a
range of clinical manifestations, including cerebellar ataxia,
epilepsy, myoclonus, choreoathetosis, and dementia. Outside the
Japanese population, the prevalence is extremely low worldwide. The
reason for different ethnic prevalences of DRPLA is unclear. A previous
assumption was that large normal alleles contribute to generation of
expanded alleles and the relative frequencies of DRPLA.
Objectives To describe the clinical, radiological, and genetic
features of the first reported Chinese family with DRPLA, to our
knowledge, and to compare the size distribution of normal alleles at
the DRPLA locus in healthy Chinese individuals with that
of other ethnic groups.
Patients and Methods Of 80 Chinese kindreds with autosomally
dominant spinocerebellar ataxias, 1 pedigree with 2 affected patients
was found by polymerase chain reaction to carry the characteristic
DRPLA mutation. The allele frequencies of different CAG
repeat lengths at the DRPLA locus in 225 healthy Chinese
individuals were also analyzed and compared with Japanese, white, and
African American distributions.
Results The clinical presentations of the 2 Chinese patients
affected with DRPLA are similar to those described in Japanese
patients, except that the affected father exhibited myoclonus but not
chorea. Although the normal DRPLA allele size is
distributed similarly in Chinese and Japanese populations, DRPLA in
Chinese individuals is rare. Thus far, to our knowledge, only 1
intermediate-sized allele containing more than 30 CAG repeats has been
reported among healthy Chinese individuals, in contrast to 3 among
Japanese populations.
Conclusion The ethnic prevalence of DRPLA seems to be
correlated with the prevalence of intermediate-sized alleles in
individual populations.
From
The Neurological Institute, Taipei Veterans General Hospital (Drs
Lee and Soong and Ms Lu), Department of Neurology,
National Yang-Ming University School of Medicine (Dr Soong),
and Department of Mathematics, Tamkang University (Dr Chang),
Taipei, Taiwan, Republic of China.
Corresponding author and reprints: Bing-Wen Soong, MD, PhD, The
Neurological Institute, Taipei Veterans General Hospital, No. 201,
Section 2, Shih-Pai Rd, Taipei, Taiwan 112, Republic of China (e-mail: bwsoong{at}vghtpe.gov.tw).
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