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Publikováno v:
Revista de Neurología. 35:131
Introduction. Schwartz-Jampel syndrome is a usually recessive disorder that presents myotonia, skeletal (bone dysplasia) and facial (blepharophimosis) anomalies and low height, which is diagnosed in childhood. We report on the clinical, electromyogra
Autor:
Carod-Artal FJ; Hospital Sarah, Brasilia DF, Brasil. javier@bsb.sarah.br, Fernandes da Silva TV, Christino-Marinho PB, Bonfim-Souza D
Publikováno v:
Revista de neurologia [Rev Neurol] 2002 Jul 16-31; Vol. 35 (2), pp. 131-4.