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. Author manuscript; available in PMC: 2009 Dec 1.
Published in final edited form as: Brain Dev. 2008 Sep 19;31(6):465–468. doi: 10.1016/j.braindev.2008.08.005

Fig. 1.

Fig. 1

(A) The patient can stand and walk with no support. Minimal calf hypertrophy is seen.

(B) T2 weighted brain magnetic resonance imaging shows no obvious brain anomaly, cortical dysplasia, or white matter changes.

(C) Sequence analysis of POMT2 revealed a homozygous mutation at c.604T>G in exon 5.