TY - JOUR
T1 - Huntington disease in subjects from an Israeli Karaite community carrying alleles of intermediate and expanded CAG repeats in the HTT gene
T2 - Huntington disease or phenocopy?
AU - Herishanu, Yuval O.
AU - Parvari, Ruti
AU - Pollack, Yaakov
AU - Shelef, Ilan
AU - Marom, Batia
AU - Martino, Tiziana
AU - Cannella, Milena
AU - Squitieri, Ferdinando
N1 - Funding Information:
We thank Y Virguin for editing assistance and all the patients for their cooperation. The financial support of Associazione Italiana Corea di Huntington (AICH) – Neuromed and of Telethon – Italy to FS (Grant no. GGP06181), is gratefully acknowledged.
PY - 2009/2/15
Y1 - 2009/2/15
N2 - We report a cluster of patients from a Karaite Jew community with a movement disorder suggestive of Huntington disease (HD), in some cases associated with repeat lengths below the edge of 36 CAG repeats. The study describes the clinical and genetic features of four patients who were followed over several years. Patients belonged to an inbred family in whom progressive chorea, manifesting predominantly with dystonia and cerebellar features, developed during middle age. Although severe psychiatric symptoms ultimately developed in two of the four patients, cognitive function remained reasonably well preserved in all of them even after several disease years. Moderate cognitive deficits were limited to the visuomotor organization and abstract thinking subtests in three of the four patients. Qualitative brain imaging showed atrophy of brain predominantly involving cortex and cerebellum. Genetic testing revealed a variable mutation penetrance among family members, some affected members showing an upper allele size ranging from 34 to 49, whereas others remained unaffected despite the presence of the full mutation beyond 40 CAG repeats. Co-morbidity with recessive hereditary inclusion body myopathy was found in two subjects from one family. Although the main diagnosis of HD remains to be confirmed by further neuropathological studies, these cases may suggest that HD could manifest with as few as 34 CAG repeats, in some geographic areas, the disease phenotype most probably being influenced by additional, as yet unidentified, genes.
AB - We report a cluster of patients from a Karaite Jew community with a movement disorder suggestive of Huntington disease (HD), in some cases associated with repeat lengths below the edge of 36 CAG repeats. The study describes the clinical and genetic features of four patients who were followed over several years. Patients belonged to an inbred family in whom progressive chorea, manifesting predominantly with dystonia and cerebellar features, developed during middle age. Although severe psychiatric symptoms ultimately developed in two of the four patients, cognitive function remained reasonably well preserved in all of them even after several disease years. Moderate cognitive deficits were limited to the visuomotor organization and abstract thinking subtests in three of the four patients. Qualitative brain imaging showed atrophy of brain predominantly involving cortex and cerebellum. Genetic testing revealed a variable mutation penetrance among family members, some affected members showing an upper allele size ranging from 34 to 49, whereas others remained unaffected despite the presence of the full mutation beyond 40 CAG repeats. Co-morbidity with recessive hereditary inclusion body myopathy was found in two subjects from one family. Although the main diagnosis of HD remains to be confirmed by further neuropathological studies, these cases may suggest that HD could manifest with as few as 34 CAG repeats, in some geographic areas, the disease phenotype most probably being influenced by additional, as yet unidentified, genes.
KW - Huntington disease mutation penetrance
KW - Huntington disease phenocopies
KW - Huntington disease pre-mutations
KW - Karaite community
KW - Movement disorder
UR - http://www.scopus.com/inward/record.url?scp=58149457367&partnerID=8YFLogxK
U2 - 10.1016/j.jns.2008.11.005
DO - 10.1016/j.jns.2008.11.005
M3 - Article
AN - SCOPUS:58149457367
VL - 277
SP - 143
EP - 146
JO - Journal of the Neurological Sciences
JF - Journal of the Neurological Sciences
SN - 0022-510X
IS - 1-2
ER -