| Title : Familial lecithin:cholesterol acyltransferase deficiency. Report of a fourth family from northwestern Norway - Gjone_1981_Acta.Med.Scand_210_3 |
| Author(s) : Gjone E , Blomhoff JP , Holme R , Hovig T , Olaisen B , Skarbovik AJ , Teisberg P |
| Ref : Acta Med Scand , 210 :3 , 1981 |
|
Abstract :
The tenth Norwegian patient with familial LCAT deficiency is reported. Her family lives in the same area as the three previously reported Norwegian families. The patient is a 26-year-old female with typical findings of the disease--proteinuria and corneal opacities. Total cholesterol was normal, but the main part was present in the free form. Triglycerides were slightly elevated. Kidney function was normal. A large molecular weight fraction of LDL was present in plasma. |
| PubMedSearch : Gjone_1981_Acta.Med.Scand_210_3 |
| PubMedID: 7293825 |
Gjone E, Blomhoff JP, Holme R, Hovig T, Olaisen B, Skarbovik AJ, Teisberg P (1981)
Familial lecithin:cholesterol acyltransferase deficiency. Report of a fourth family from northwestern Norway
Acta Med Scand
210 :3
Gjone E, Blomhoff JP, Holme R, Hovig T, Olaisen B, Skarbovik AJ, Teisberg P (1981)
Acta Med Scand
210 :3