Charcot-Marie-Tooth neuropathy type 1 (CMT1), the most common hereditary neurological disorder in humans, is characterized by clinical and genetic heterogeneity. It is caused mainly by a 1.5 Mb duplication in 17p11.2, but also by mutations in the myelin genes PMP22 (peripheral myelin protein 22), MPZ (myelin protein zero), Cx32 (connexin 32; also called GJB1), and EGR2 (early growth response 2). In this study, we have screened 172 index cases of Italian families in which there was at least one subject with a CMT1 diagnosis for the duplication on 17p11.2 and mutations in these genes. Among 170 informative unrelated patients, the overall duplication frequency was 57.6%. A difference could be observed between the duplication frequency in familial cases (71.6%) and that observed in non-familial cases (36.8%). Among the non-duplicated patients, 12 were mutated in Cx32, four in MPZ, two in PMP22, and none in the EGR2. In the non-duplicated cases, the overall point mutation frequency for these genes was 25.0%. We describe the mutations identified, and consider possible genotype-phenotype correlation.
|Autori interni:||SICILIANO, GABRIELE|
|Autori:||MOSTACCIOLO ML; RIGHETTI E; ZORTEA M; BORSELLO V; SCHIAVON F; VALLO L; MERLINI L; SICILIANO G; FABRIZI GM; RIZZUTO N; DILANI M; BARATTA S; TAVONI F|
|Titolo:||Charcot-marie-tooth disease type 1 and related demyelinating neuropathies: mutation analysis in a large cohort of italian families|
|Anno del prodotto:||2001|
|Appare nelle tipologie:||1.1 Articolo in rivista|