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. 2009 Oct 29;94(12):4971–4983. doi: 10.1210/jc.2009-0472

Figure 1.

Figure 1

Patients with APS. A, A 13-yr-old girl (APS 700.4) with Henoch-Schonlein purpura, spondylolisthesis, and avascular necrosis of right hip joint, dysplasia of heart valves, alopecia, and E159K mutation. B, A 27-yr-old woman (APS 200.5) with generalized lipodystrophy, diabetes, hypertriglyceridemia, and D136H mutation. C, A 16-yr-old female (APS 600.3) with diabetes, partial lipodystrophy and C588R mutation. D, A 51-year-old woman (APS 300.3) with partial lipodystrophy, diabetes, valvular anomalies, telangiectasias of the skin, and P4R mutation. E, Telangiectasias on the abdomen in a 51-yr-old woman (APS 300.3) with P4R mutation. F, A 7-yr-old boy (APS 400.5) with axillary freckles and C588R mutation.