Lattice Corneal Dystrophy Type 1
What's New
Last Posted: Mar 10, 2023
- Prevalence of transforming growth factor ?-induced gene corneal dystrophies in Chinese refractive surgery candidates.
Song Yanzheng, et al. Journal of cataract and refractive surgery 2017 0 (12) 1489-1494 - Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6.
Yaylacioglu Tuncay Fulya, et al. Molecular vision 2016 0 1267-1279 - Lattice corneal dystrophy type 1
From NCATS Genetic and Rare Diseases Information Center - Lattice corneal dystrophy type 3A
From NCATS Genetic and Rare Diseases Information Center - An R124C mutation in TGFBI caused lattice corneal dystrophy type I with a variable phenotype in three Chinese families.
Liu Zhe, et al. Molecular vision 2008 0 1234-9
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Feb 1, 2024
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