A Case of Familial Lecithin-cholesterol Acyltransferase (LCAT) Deficiency
Journal of the Korean Ophthalmological Society
;
: 831-834, 2008.
Artigo
em Coreano
| WPRIM
| ID: wpr-82148
ABSTRACT
PURPOSE:
To report a case of a familial lecithin cholesterol acyltransferase (LCAT) deficiency patient with bilateral corneal opacities. CASESUMMARY:
A 26-year-old man with bilateral corneal opacities visited our hospital. We took slit lamp examination, corneal thickness measurement, corneal endothelial cell counts and fundus examination. Blood and urine tests were included. Kidney biopsy was done. The tissues were observed by a light microscopy and an electron microscopy. Hemolytic anemia, proteinuria, hematuria, hypertriglyceridemia, decreased HDL cholesterol level, and lecithin cholesterol acyltransferase (LCAT) deficiency were found. At kidney biopsy, electron-lucent vacuoles and lamellar inclusion body were found.CONCLUSIONS:
Bilateral corneal opacities can be an imporant clinical sign of systemic disease which is caused by abnormal lipid metabolism like the familial lecithin cholesterol acyltransferase (LCAT) deficiency.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Proteinúria
/
Vacúolos
/
Biópsia
/
Microscopia Eletrônica
/
Hipertrigliceridemia
/
Corpos de Inclusão
/
Opacidade da Córnea
/
Células Endoteliais
/
Metabolismo dos Lipídeos
/
Paquimetria Corneana
Limite:
Adulto
/
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Ano de publicação:
2008
Tipo de documento:
Artigo
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