Serial Observations and Mutational Analysis of an Adoptee with Family History of Hypertrophic Cardiomyopathy
Figure 1
Pedigree of the adoptee. The proband is highlighted by the arrow. The proband carries two sequence variations within the MYH7 (cardiac beta-myosin heavy chain gene): 2156GA (R719Q) change in exon 19 (marked by a shaded area on upper left hand corner), and 4537AT (T1513S) on exon 33 (the shaded area on the lower left hand corner). Cardiac hypertrophy is marked by shaded area on upper right-hand corner). SCD: sudden cardiac death. ICD: internal cardiac defibrillator placed (dot).