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Crisponi syndrome: report of a further patient
P Accorsi1, L Giordano, F Faravelli
1Divisione di Neuropsichiatria Infantile, A.O. Spedali Civili di Brescia, Piazzale Spedali Civili, 25123 Brescia, Italy. pafivan@libero.it
American Journal of Medical Genetics. Part A
|November 5, 2003
Abstract:
Crisponi syndrome was described in the original paper in 17 patients form 12 families [Crisponi, 1996: Am J Med Genet 62:365-371]. It is characterised by episodes of muscle contraction in response to external stimuli and intermittent hypethermia with neonatal onset. The disease is often lethal in the first infancy. We describe a patient with the same unusual phenotype.