Lecithin cholesterol acyltransferase deficiency: A case report of corneal histopathology and review of family history

Keyphrases

• 50 Years Old 25%
• Activity Value 25%
• Acyl Transfer 100%
• Anemia 25%
• Autosomal Dominant 25%
• Biopsy Specimen 50%
• Clinical Characteristics 25%
• Clinical Tissues 25%
• Corneal Abnormalities 25%
• Corneal Haze 25%
• Corneal Histopathology 100%
• Corneal Opacification 75%
• Corneal Stroma 25%
• Electron Microscopic Study 25%
• Electron Microscopy 25%
• Electron-dense Deposits 25%
• Eye Examination 25%
• Family Health History 25%
• Family History 100%
• Family Members 50%
• Genetic Transmission 25%
• Kidney Biopsy 25%
• Lecithin-cholesterol Acyltransferase 100%
• Lecithin-cholesterol Acyltransferase Deficiency 100%
• Mild Renal Insufficiency 25%
• Obligate Carrier 25%
• Older Women 25%
• Penetrating Keratoplasty 25%
• Pseudoautosomal 25%
• Renal Biopsy 25%
• Renal Disease 50%
• Stromal Dystrophy 25%
• Tissue Pathology 25%
• Visual Acuity 25%

Medicine and Dentistry

• Anemia 25%
• Autosomal Dominant Inheritance 25%
• Biopsy Sample 50%
• Disease 25%
• Dystrophy 25%
• Electron Microscopy 25%
• Eye Examination 25%
• Family History 100%
• Histopathology 100%
• Hyperlipidemia 50%
• Lecithin Cholesterol Acyltransferase Deficiency 100%
• Mild Renal Impairment 25%
• Obligate Carrier 25%
• Penetrating Keratoplasty 25%
• Phosphatidylcholine Sterol Acyltransferase 100%
• Renal Biopsy 50%
• Stroma of Cornea 25%
• Visual Acuity 25%