Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery-Dreifuss muscular dystrophy patients and carriers

被引:31
作者
Sabatelli, P
Squarzoni, S
Petrini, S
Capanni, C
Ognibene, A
Cartegni, L
Cobianchi, F
Merlini, L
Toniolo, D
Maraldi, NM
机构
[1] IOR, CNR, Ist Citomorfol NP, Bologna, Italy
[2] IOR, Lab Patol Neuromuscolare, Bologna, Italy
[3] Univ Bologna, Dipartimento Biochim G Moruzzi, Bologna, Italy
[4] IOR, Lab Biol Cellualare & Microscopia Elettron, Bologna, Italy
[5] CNR, Ist Genet Biochim & Evoluzionist, I-27100 Pavia, Italy
关键词
Emery-Dreifuss muscular dystrophy (EMD); emerin; immunohistochemistry; SDS-polyacrylamide gel electrophoresis (SDS-PAGE); immunoblotting;
D O I
10.1016/S0960-8966(97)00147-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Emery-Dreifuss muscular dystrophy (EMD) is an inherited myopathy characterised by muscle contractures, progressive muscle wasting and weakness, with humeroperoneal distribution. Cardiac arrhythmia and heart conduction block are also important characteristics of this disease. The X-linked form of EMD is caused by the absence of emerin, encoded by the STA gene (Xq28), Emerin is normally localised in muscle and other tissues at the nuclear rim. Currently, muscle and skin biopsies are used for the immunohistochemical diagnosis. We demonstrate that emerin is present in the cheek oral mucosa, in the exfoliating epithelial cells, and we propose the collection of these cells as a new method for the diagnosis of X-linked EMD patients and the detection of carriers by immunofluorescence techniques: smears from healthy subjects contained about 98% emerin-positive cells, those from X-linked EMD patients contained none and those from carriers contained about 45%. The technique is completely non-invasive, simple, repeatable and inexpensive. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:67 / 71
页数:5
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