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Congenital muscular dystrophy type 1A with residual merosin expression

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Fig. 1.  Axial T2-weighted brain magnetic resonance images of the patient at 6 months of age shows  high signal intensity in the white matter of the peritrigone and external capsule (A); slight progression of  dysmyelination can be seen 2 months later (B).
Fig. 3.  Immunohistochemical staining of the patient’s muscle fiber demonstrates partially decreased laminin  α 2  expression (A, ×400) comparing with normal expression of dystrophin (B, ×400) and  α -dystroglycan (C, ×400).

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