Different phenotypes in identical twins with cerebrotendinous xanthomatosis case series /
Cerebrotendinous xanthomatosis (CTX) is a rare, genetically determined error of metabolism. The characteristic clinical symptoms are diarrhea, juvenile cataracts, tendon xanthomas and neuropsychiatric alterations. The aim of this study is to present a pair of identical adult twins with considera...
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| Dokumentumtípus: | Cikk |
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Springer-Verlag
2017
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| Sorozat: | NEUROLOGICAL SCIENCES
38 No. 3 |
| doi: | 10.1007/s10072-016-2776-6 |
| mtmt: | 3147588 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/11682 |
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| 024 | 7 | |a 10.1007/s10072-016-2776-6 |2 doi | |
| 024 | 7 | |a 3147588 |2 mtmt | |
| 040 | |a SZTE Publicatio Repozitórium |b hun | ||
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| 100 | 1 | |a Zádori Dénes | |
| 245 | 1 | 0 | |a Different phenotypes in identical twins with cerebrotendinous xanthomatosis |h [elektronikus dokumentum] : |b case series / |c Zádori Dénes |
| 260 | |a Springer-Verlag |c 2017 | ||
| 300 | |a 481-483 | ||
| 490 | 0 | |a NEUROLOGICAL SCIENCES |v 38 No. 3 | |
| 520 | 3 | |a Cerebrotendinous xanthomatosis (CTX) is a rare, genetically determined error of metabolism. The characteristic clinical symptoms are diarrhea, juvenile cataracts, tendon xanthomas and neuropsychiatric alterations. The aim of this study is to present a pair of identical adult twins with considerable differences in the severity of phenotype. With regards to neuropsychiatric symptoms, the predominant features were severe Parkinsonism and moderate cognitive dysfunctions in the more-affected individual, whereas these alterations in the less-affected patient were only very mild and mild, respectively. The characteristic increase in the concentrations of serum cholestanol and the lesion volumes in dentate nuclei in the brain assessed with magnetic resonance imaging were quite similar in both cases. The lifestyle conditions, including eating habits of the twin pair, were quite similar as well; therefore, currently unknown genetic modifiers or certain epigenetic factors may be responsible for the differences in severity of phenotype. This case series serves as the first description of an identical twin pair with CTX presenting heterogeneous clinical features. | |
| 700 | 0 | 1 | |a Szpisjak László |e aut |
| 700 | 0 | 1 | |a Madar László |e aut |
| 700 | 0 | 1 | |a Varga Viktória Evelin |e aut |
| 700 | 0 | 1 | |a Csányi Bernadett |e aut |
| 700 | 0 | 1 | |a Bencsik Krisztina |e aut |
| 700 | 0 | 1 | |a Balogh István |e aut |
| 700 | 0 | 1 | |a Harangi Mariann |e aut |
| 700 | 0 | 1 | |a Kereszty Éva Margit |e aut |
| 700 | 0 | 1 | |a Vécsei László |e aut |
| 700 | 0 | 1 | |a Klivényi Péter |e aut |
| 856 | 4 | 0 | |u http://publicatio.bibl.u-szeged.hu/11682/1/Zadori_D._NEUS_D_16_00859_R1_u_.pdf |z Dokumentum-elérés |
| 856 | 4 | 0 | |u http://publicatio.bibl.u-szeged.hu/11682/7/Neurol_sci_2017_3_tartj.pdf |z Dokumentum-elérés |