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Strio-pallido-dentate calcinosis: a diagnostic approach in adult patients

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Abstract

Familial idiopathic bilateral strio-pallido-dentate calcinosis is a rare autosomal dominant disorder characterized by massive symmetric calcification, detectable by CT, into the globus pallidus and striatum, with or without the involvement of the dentate nucleus, thalamus and white matter in the absence of alterations of calcium metabolism. Clinically, it has been associated with movement and/or neuropsychiatric disorders with age at onset typically in the fourth or fifth decade. Other sporadic or familial diseases can be responsible for brain calcifications with a similar anatomic strio-pallidal or strio-pallido-dentate pattern and, a restricted number of them, for neurological symptoms with onset in adulthood. Moreover, physiological age-related basal ganglia calcifications are often incidentally found, although with a far different CT aspect, in elderly patients with movement disorders. Indentifying familial and idiopathic cases may offer the opportunity to study the molecular mechanisms underlying this minerals deposition.

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  1. Dipartimento di Scienze Neurologiche, Università di Bologna, Via Foscolo 7, 40123, Bologna, Italy

    Sara Bonazza, Chiara La Morgia, Paolo Martinelli & Sabina Capellari

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  1. Sara Bonazza
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  2. Chiara La Morgia
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Correspondence to Paolo Martinelli.

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Bonazza, S., La Morgia, C., Martinelli, P. et al. Strio-pallido-dentate calcinosis: a diagnostic approach in adult patients. Neurol Sci 32, 537–545 (2011). https://doi.org/10.1007/s10072-011-0514-7

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