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Fig. 1 | Journal of Medical Case Reports

Fig. 1

From: Carnitine palmitoyltransferase type 2 deficiency: novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: two case reports

Fig. 1

Whole-body magnetic resonance imaging T1-weighted axial sections in both siblings (1a and 1b: boy; 2a–2d: girl). Involved muscles are depicted by black arrows. 1a and 2a: Mild hypersignal of thoracic extensors. 1b and 2b: Mild hypersignal of tensor fasciae latae and gluteus maximus. 2c: Sartorius mild hypersignal. 2d: Soleus mild hypersignal and medial gastrocnemius atrophy

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Journal of Medical Case Reports

ISSN: 1752-1947