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. 2023 Apr 21;25(Suppl B):B7–B11. doi: 10.1093/eurheartjsupp/suad059

Figure 1.

Figure 1

The figure includes a table (A) and a graphical view (B) of the number and PMID of scientific reports describing genetic defects identified in spontaneous coronary artery dissection. Numbers in PMID columns refer to the number of reported cases. Genes reported more than once include COL3A1, SMAD3, FBN1, COL4A1, PKD1, LOX, and TGFBR2. Other genes are reported once but are well known to be associated with syndromic and non-syndromic connective tissue diseases and include TGFB2, TGFB3, MYLK, SMAD2, COL4A5, LMX1B, ALDH18A1, ACVR1, AEBP1, SCL2A10, ABCC6, YY1AP1, FLNA, and PRKG1. Other genes (TSR1 and TLN1) are provisional and still unconfirmed.