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Figure 1 | Orphanet Journal of Rare Diseases

Figure 1

From: Guidelines for the diagnosis and management of chylomicron retention disease based on a review of the literature and the experience of two centers

Figure 1

Etiology of familial hypocholesterolemia in childhood depending on lipid profile. ABL, abetalipoproteinemia; AD, autosomal dominant; AR, autosomal recessive; apo AI, apolipoprotein A1; apo B; apolipoprotein B; HDL, high-density lipoprotein; HBL, hypobetalipoproteinemia; LCAT, lecithin cholesterol acyltransferase; LDL, low-density lipoprotein; MTP, microsomal triglyceride transfer protein; N, normal; 0, nul; PL, phospholipids; TC, total cholesterol; CRD, chylomicron retention disease; TG, triglyceride; ↓, few decrease; ↓↓, significant decrease; ↓↓↓, intense decrease.

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172