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. Author manuscript; available in PMC: 2020 Jan 5.
Published in final edited form as: J Clin Lipidol. 2008 Jun 13;2(4):237–247. doi: 10.1016/j.jacl.2008.06.002

Figure 1.

Figure 1

(A) Tubero-eruptive xanthomas on the buttocks of a patient with homozygous familial apolipoprotein A-I deficiency as described in Matsunaga and colleagues.28 (B) Light microscopy of a biopsy of one of these xanthomas documenting lipid-laden macrophages. (C) Planar xanthomas in the skin creases of the wrist. (D) Photograph of the eye of a patient with homozygous familial apolipoprotein A-I deficiency as described in Santos and colleagues,31 documenting moderate corneal opacification, especially in the limbic area, and (E) fundus of the same patient with no significant abnormalities noted.

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