Background: A complicated form of recessive hereditary spastic paraplegias (HSPs) with thin corpus callosum (TCC) was first described in Japan, and most of the Japanese families showed linkage to chromosome 15q13-15. A recessive HSP locus (SPG11) has also been mapped to chromosome 15q13-15 in Italian and North American families with and without TCC, and it overlaps the region identified in the Japanese families. Objective: To study clinically and genetically 12 Italian families with HSP and TCC. Methods: The authors investigated 18 affected and 30 healthy individuals from 12 unrelated Italian families with recessive HSP-TCC. Clinical, neurophysiologic, and neuroradiologic studies were undertaken. All patients were negative for SPG7 mutations. Genetic linkage analyses were carried out with polymorphic DNA markers on 15q13-15. Results: Five families were consistent with linkage, thus defining a 19.8-cM region between markers D15S1007 and D15S978, encompassing the SPG11 interval. In one consanguineous family, linkage could be firmly excluded, confirming genetic heterogeneity. Two families appeared not linked to the region, but this could not be firmly proved because of the small family size. The remaining four families were uninformative for linkage purposes. Conclusion: HSP-TCC is common in Italy. The phenotype is fairly homogeneous and is associated with impaired cognition. There are at least two loci for HSP-TCC, one of which is on chromosome 15q13-15.

Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum / Casali, Carlo; E. M., Valente; E., Bertini; G., Montagna; C., Criscuolo; G., De Michele; M., Villanova; M., Damiano; Pierallini, Alberto; Francesco, Brancati; V., Scarano; A., Tessa; F., Cricchi; G. S., Grieco; M., Muglia; M., Carella; B., Martini; A., Rossi; Amabile, Giuseppe Amadio; Nappi, Giuseppe; A., Filla; DALLA PICCOLA, Bruno; F. M., Santorelli. - In: NEUROLOGY. - ISSN 0028-3878. - 62:2(2004), pp. 262-268.

Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum

CASALI, Carlo;PIERALLINI, Alberto;AMABILE, Giuseppe Amadio;NAPPI, Giuseppe;DALLA PICCOLA, Bruno;
2004

Abstract

Background: A complicated form of recessive hereditary spastic paraplegias (HSPs) with thin corpus callosum (TCC) was first described in Japan, and most of the Japanese families showed linkage to chromosome 15q13-15. A recessive HSP locus (SPG11) has also been mapped to chromosome 15q13-15 in Italian and North American families with and without TCC, and it overlaps the region identified in the Japanese families. Objective: To study clinically and genetically 12 Italian families with HSP and TCC. Methods: The authors investigated 18 affected and 30 healthy individuals from 12 unrelated Italian families with recessive HSP-TCC. Clinical, neurophysiologic, and neuroradiologic studies were undertaken. All patients were negative for SPG7 mutations. Genetic linkage analyses were carried out with polymorphic DNA markers on 15q13-15. Results: Five families were consistent with linkage, thus defining a 19.8-cM region between markers D15S1007 and D15S978, encompassing the SPG11 interval. In one consanguineous family, linkage could be firmly excluded, confirming genetic heterogeneity. Two families appeared not linked to the region, but this could not be firmly proved because of the small family size. The remaining four families were uninformative for linkage purposes. Conclusion: HSP-TCC is common in Italy. The phenotype is fairly homogeneous and is associated with impaired cognition. There are at least two loci for HSP-TCC, one of which is on chromosome 15q13-15.
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Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum / Casali, Carlo; E. M., Valente; E., Bertini; G., Montagna; C., Criscuolo; G., De Michele; M., Villanova; M., Damiano; Pierallini, Alberto; Francesco, Brancati; V., Scarano; A., Tessa; F., Cricchi; G. S., Grieco; M., Muglia; M., Carella; B., Martini; A., Rossi; Amabile, Giuseppe Amadio; Nappi, Giuseppe; A., Filla; DALLA PICCOLA, Bruno; F. M., Santorelli. - In: NEUROLOGY. - ISSN 0028-3878. - 62:2(2004), pp. 262-268.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/365430
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