features
autosomal dominant
low HDL, apo1
decreased LDL
mildly increased TG
mutations in binding cassette transporter A1 (ABDA1)
abnormal reverse cholesterol transport
orange tonsils
peripheral neuropathy
cerebrovascular and cardiovascular disease.
autosomal dominant
low HDL, apo1
decreased LDL
mildly increased TG
mutations in binding cassette transporter A1 (ABDA1)
abnormal reverse cholesterol transport
orange tonsils
peripheral neuropathy
cerebrovascular and cardiovascular disease.
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