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Bietti Crystalline Dystrophy

A rare hereditary form of retinal degeneration that occurs more frequently in persons of East Asian descent. Inheritance is autosomal recessive and onset is typically in young adulthood. It is characterized by the accumulation of numerous lipid vesicles over the FUNDUS OCULI; SCLEROSIS of the CHORIOID vessels, progressive NIGHT BLINDNESS, and constriction of the VISUAL FIELDS. Mutations in the CYP4V2 gene have been identified. OMIM: 210370
Also Known As:
Bietti Crystalline Corneoretinal Dystrophy; Bietti Crystalline Retinopathy; Bietti tapetoretinal degeneration with marginal corneal dystrophy; Bietti's crystalline corneoretinal dystrophy; Bietti's crystalline dystrophy
Networked: 60 relevant articles (0 outcomes, 4 trials/studies)

Disease Context: Research Results

Related Diseases

1. Retinal Diseases
2. Leber Congenital Amaurosis
3. Choroideremia
4. Diabetic Retinopathy (Retinopathy, Diabetic)
5. Atrophy

Experts

1. Yoshimura, Nagahisa: 4 articles (10/2018 - 03/2012)
2. Gotoh, Norimoto: 3 articles (10/2018 - 01/2016)
3. Hata, Masayuki: 3 articles (10/2018 - 01/2016)
4. Kelly, Edward J: 3 articles (01/2018 - 11/2009)
5. Rettie, Allan E: 3 articles (01/2018 - 11/2009)
6. Ogino, Ken: 3 articles (06/2017 - 03/2012)
7. Sui, Ruifang: 2 articles (01/2022 - 01/2020)
8. Sun, Zixi: 2 articles (01/2022 - 01/2020)
9. Wu, Shijing: 2 articles (01/2022 - 01/2020)
10. Zou, Xuan: 2 articles (01/2022 - 01/2020)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Bietti Crystalline Dystrophy:
1. Retinaldehyde (Retinal)IBA
2. Proteins (Proteins, Gene)FDA Link
3. Green Fluorescent ProteinsIBA
4. Nonsense Codon (Nonsense Mutation)IBA
5. TransferasesIBA
6. Isoflurophate (DFP)FDA Link
7. Hydroxymethylglutaryl CoA Reductases (HMG CoA Reductase)IBA
8. Coenzyme A (CoA)IBA
9. cytotropic heterogeneous molecular lipid (CHML)IBA
10. Rab geranylgeranyl transferase beta-subunitIBA

Therapies and Procedures

1. Intravitreal Injections
2. Light Coagulation
3. Lasers (Laser)
4. Injections