A 13-Year-Old Boy from Thailand with Hutchinson-Gilford Progeria Syndrome with Coronary Artery and Aortic Calcification and Non-ST-Segment Elevation Myocardial Infarction (NSTEMI)

Natnicha Pongbangli; Kannika Pitipakorn; Sasivimon Jai-aue; Piyaporn Sirijanchune; Sorawit Pongpittayut; Wanwarang Wongcharoen

doi:10.12659/AJCR.928969

08 January 2021 : Case report Thailand

A 13-Year-Old Boy from Thailand with Hutchinson-Gilford Progeria Syndrome with Coronary Artery and Aortic Calcification and Non-ST-Segment Elevation Myocardial Infarction (NSTEMI)

Rare disease

Natnicha Pongbangli^1ABDEF*, Kannika Pitipakorn^2BDE, Sasivimon Jai-aue^1BDE, Piyaporn Sirijanchune^3BEF, Sorawit Pongpittayut^2BDE, Wanwarang Wongcharoen^4EF

DOI: 10.12659/AJCR.928969

Am J Case Rep 2021; 22:e928969

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Figure 1. The patient was characteristically prematurely aged, with short stature, and prominent eyes, a small chin, total alopecia, and protruding ears. The cutaneous findings of this patient demonstrated scleroderma-like skin changes and a loss of subcutaneous fat.

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A 13-Year-Old Boy from Thailand with Hutchinson-Gilford Progeria Syndrome with Coronary Artery and Aortic Calcification and Non-ST-Segment Elevation Myocardial Infarction (NSTEMI)

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