Neuroepidemiology · 2002 · 31 citations · 15 references
Genetic DisorderCharcot-marie-tooth DiseaseGeneticsPathogenesisGenetic EpidemiologyPathologyStatistical GeneticsDental DiseaseEpidemiological StudyGenetic VariationPublic HealthCmt Type 1AMedicineEpidemiologyUnrelated FamiliesCentral-southern Region
An epidemiological survey of Charcot-Marie-Tooth disease (CMT) was conducted in Molise, a central-southern region of Italy, from March 1998 to June 2000. Fifty-eight cases of CMT in 13 unrelated families were identified within the selected area. The prevalence of all subtypes of CMT was 17.5/100,000. All families underwent a bio-molecular analysis to disclose the duplication at gene locus 17p11.2 in order to ascertain the diagnosis of CMT type 1A. Our data revealed that 64% of all the observed patients had CMT1A, thus confirming the high prevalence of duplication of the 17p11.2 locus.
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DNA duplication associated with Charcot-Marie-Tooth disease type 1A
James R. Lupski, Roberto Montes‐de‐Oca‐Luna, Susan Slaugenhaupt et al. · Cell · 1991 · 1.3K citations
Genetic and clinical aspects of Charcot‐Marie‐Tooth's disease
H. Skre · Clinical Genetics · 1974 · 897 citations
THE CLINICAL FEATURES OF HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPES I AND II
A E Harding, P. K. Thomas · Brain · 1980 · 825 citations