Different phenotypes in identical twins with cerebrotendinous xanthomatosis: case series

Zádori, Dénes and Szpisjak, László and Madar, László and Varga, Viktória Evelin and Csányi, Bernadett and Bencsik, Krisztina and Balogh, István and Harangi, Mariann and Kereszty, Éva and Vécsei, László and Klivényi, Péter (2017) Different phenotypes in identical twins with cerebrotendinous xanthomatosis: case series. NEUROLOGICAL SCIENCES, 38 (3). pp. 481-483. ISSN 1590-1874

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Abstract

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.

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