Literature DB >> 22079340

Multi-organ investigation in 16 CADASIL families from central Italy sharing the same R1006C mutation.

Michele Ragno1, Luigi Pianese, Gabriella Cacchiò, Antonio Manca, Maria Scarcella, Serena Silvestri, Fabio Di Marzio, Anna Rita Caiazzo, Flavia Silvaggio, Giorgio Tasca, Massimiliano Mirabella, Luigi Trojano.   

Abstract

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) may involve many target organs with relevant variability among affected individuals. We performed a multi-organ assessment tapping nervous system, skeletal muscle and cardiovascular system in thirty-nine individuals belonging to 16 families from Central Italy sharing the same R1006C CADASIL mutation. Stroke prevalence was larger in female patients (66.7%) than in males (23.8%); high levels of CKemia were quite frequent (21.6%) and were related to a myopathy without mitochondrial alterations; several individuals had atrial septal aneurysm (10.3%). No specific relationships between common cardiovascular risk factors and clinical manifestations were found. The present systematic study thus identified several gender-related, myopathic and cardiovascular peculiarities of R1006C mutation. This kind of comprehensive approach is necessary to define clinical course, prognosis and treatment options for a multi-organ disease such as CADASIL.
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

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Year:  2011        PMID: 22079340     DOI: 10.1016/j.neulet.2011.10.062

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  2 in total

1.  Parkinsonism in a pair of monozygotic CADASIL twins sharing the R1006C mutation: a transcranial sonography study.

Authors:  Michele Ragno; Sandro Sanguigni; Antonio Manca; Luigi Pianese; Cristina Paci; Alfonso Berbellini; Valeria Cozzolino; Roberto Gobbato; Silvio Peluso; Giuseppe De Michele
Journal:  Neurol Sci       Date:  2016-02-05       Impact factor: 3.307

2.  "CADASIL coma" in an Italian homozygous CADASIL patient: comparison with clinical and MRI findings in age-matched heterozygous patients with the same G528C NOTCH3 mutation.

Authors:  Michele Ragno; Luigi Pianese; Manrico Morroni; Gabriella Cacchiò; Antonio Manca; Fabio Di Marzio; Serena Silvestri; Cristina Miceli; Maria Scarcella; Marco Onofrj; Luigi Trojano
Journal:  Neurol Sci       Date:  2013-04-10       Impact factor: 3.307

  2 in total

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