Keratoconus
What's New
Last Posted: Sep 02, 2024
- Gene?Environment Interaction Between CAST Gene and Eye-Rubbing in the Chinese Keratoconus Cohort Study: A Case-Only Study.
Shanshan Yin, et al. Investigative ophthalmology & visual science 2024 0 (10) 36 - A novel variant in the keratin 12 gene in a four-generation Chinese family with high myopia.
Qinghong Lin, et al. Eye (London, England) 2024 0 - Whole-exome sequencing screening for candidate genes and variants associated with primary sporadic keratoconus in Chinese patients.
Chunyuan Song, et al. Experimental eye research 2024 0 109978 - Association of Novel Loci With Keratoconus Susceptibility in a Chinese Genome-Wide Association Study.
Liyan Xu, et al. Investigative ophthalmology & visual science 2024 0 (5) 29 - Targeted next-generation sequencing analysis in Italian patients with keratoconus.
Marco Lombardo, et al. Eye (London, England) 2024 0 - Genetic variants in the FOXO1 and ZNF469 genes are associated with keratoconus in Sweden: a case-control study.
Wolf Wonneberger, et al. BMC ophthalmology 2024 0 (1) 36 - Association between Polymorphism rs61876744 in PNPLA2 Gene and Keratoconus in a Saudi Cohort.
Altaf A Kondkar, et al. Genes 2023 0 (12) - Impact of a 50bp insertion/deletion polymorphism of the superoxide dismutase-1 on oxidative stress status and risk of keratoconus.
Mohammad-Reza Sedaghat, et al. Experimental eye research 2023 0 109742 - Identification of genetic variants in two families with Keratoconus.
Qinghong Lin, et al. BMC medical genomics 2023 0 (1) 299 - Mitochondrial DNA heteroplasmy analysis in keratoconus patients from China.
Liyan Xu, et al. Frontiers in genetics 2023 0 1251951
More
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
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
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Content source: