Very low levels of high density lipoprotein cholesterol in four sibs of a family with non-neuropathic Niemann-Pick disease and sea-blue histiocytosis.

Author:

Viana M B,Giugliani R,Leite V H,Barth M L,Lekhwani C,Slade C M,Fensom A

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference26 articles.

1. The syndrome of the sea-blue histiocyte;Silverstein, M.N.; Ellefson, R.D.; Ahern, E.J.;N Engl J Med,1970

2. The sea-blue histiocyte syndrome with hepatic porphyria and infectious mononucleosis;Ghosh, M.L.;J Clin Pathol,1972

3. Sea-blue histiocytes in fambilirubin concentration, as liver dysfunction progresses.26 The triglyceridaemia was only modesdy ilial lecithin: cholesterol-acyl-transferase deficiency;Jacobsen, C.D.; Gjone, E.; Hovig, T.;Scand J Haematol,1972

4. Sheets RF, Fisher IK. The sea-blue histiocyte raised in three out of four sibs. In patient 3 (table 1) the value was normal and the simultaneous HDL (SBH) viewed as a definitive cell unable to process erythrocyte lipid-a morphologic study;Hamilton, H.E.;J Lab Clin Med,1971

5. Acquired lipidosis: Gaucher-like cholesterol concentration was very low (8-6 mg/dl). It is noteworthy that in two other lysosomal storage diseases low serum HDL cholesterol concentration may be found. Five patients with Gaucher's disease were reported to have values that ranged from 15 to 30 cells and 'blue cells' in chronic granulocytic leukemia;Dosik, H.; Rosner, F.; Sawitsky, A.;Semin Hematol,1972

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