Sinus Node Disease And Myopia

Watchlist

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Retrieved

2019-09-22

Source

Omim

Trials

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Genes

MYH6, SCN5A, HCN4, POMC, CACNA1D, KCNJ5, HCN1, SCN10A, CACNA1C, KCNE5, GPD1L, GNB5, AKAP9, PKP2, RANGRF, KCNE3, SLMAP, TRPM4, SCN3B, SCN1B, SGO1, ABCC9, SCN2B, CACNA2D1, KCNJ8, CACNB2, CALM2, KCND3, MECP2, PDCD1, ICAM1, TRPM7, COL1A2, TXN2, CCN2, FBN1, FGFR3, FN1, IL6, IGF1, MEF2C, HDAC4, TBX18, VEGFA, VCAM1, TTN, THBS1, TGFB1, CCL2, LMNA, AGT

Drugs

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See 163800 for a discussion of disturbance of the sinoatrial node, including the so-called sick sinus syndrome (SSS). Onat (1986) described SSS in father, daughter and son. The 2 elder affected persons had severe degenerative myopia. It was suggested that the youngest affected person, still under age 7 years, might develop this feature.