Tangier disease

Tangier disease (TD) is a rare lipoprotein metabolism disorder characterized biochemically by an almost complete absence of plasma high-density lipoproteins (HDL), and clinically by liver, spleen, lymph node and tonsil enlargement along with peripheral neuropathy in children and adolescents, and, occasionally, cardiovascular disease in adults.

Also known as: ATP-binding cassette transporter A1 deficiency, Analphalipoproteinemia, Tangier disease, defective adenosine triphosphate-binding cassette transporter A1, A-alphalipoprotein neuropathy, Alpha high density lipoprotein deficiency disease, Analphalipo-proteinemia, HDL lipoprotein deficiency disease

0 clinical trials for this condition and its sub-types, 0 tagged with Tangier disease itself.