Lattice corneal dystrophy, gelsolin type (Meretoja’s syndrome)

. Purpose: This paper reviews current knowledge about the pathogenesis, clinical manifestations and treatment of lattice corneal dystrophy, gelsolin type (LCD2, Meretoja’s syndrome). Methods: Material is derived from literature searches, a case study of a Finnish patient living in Sweden, and inte...

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Veröffentlicht in:	Acta ophthalmologica (Oxford, England) England), 2009-12, Vol.87 (8), p.813-819
Hauptverfasser:	Carrwik, Christian, Stenevi, Ulf
Format:	Artikel
Sprache:	eng
Schlagworte:	amyloidosis Cataract - etiology Cornea - pathology Corneal Dystrophies, Hereditary - complications Corneal Dystrophies, Hereditary - diagnosis Corneal Dystrophies, Hereditary - drug therapy Corneal Dystrophies, Hereditary - physiopathology Eye Facies familial amyloidosis Female Gelsolin - genetics gelsolin type Glaucoma - etiology Humans Intraocular Pressure Kidney Diseases - etiology lattice corneal dystrophy LCD2 Lubricants - therapeutic use Meretoja’s syndrome Middle Aged Mutation Nervous System Diseases - etiology Pedigree Skin Diseases - etiology Sleep Apnea Syndromes - etiology
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