Fig.2
From: Beware of missed diagnosis in patients with multiple genetic diseases: a case report
Pedigree chart. The father (I1) was healthy (marked as a hollow square). The mother (I2) was healthy (marked as a black dot in a circle) even though she carried a repeat of exon 3 to exon 9 of the DMD. The patient (II1, pointed out by the arrow) inherited the variant from his mother and carried another de novo variant, a heterozygous nonsense mutation c.418G > T in exon 6 of PDCD10, and the patient developed DMD and CCMs (marked as half dark and half shadow)