Papilledema
What's New
Last Posted: Mar 04, 2023
- Role of ultrasonographic optic nerve sheath diameter in the diagnosis and follow-up of papilledema and its correlation with Frisén's severity grading.
Raghunandan Nithya, et al. Indian journal of ophthalmology 2019 0 (8) 1310-1313 - Atypical Ocular Coloboma in Tuberous Sclerosis-2: Report of Two Novel Cases.
Bacci Giacomo M, et al. Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society 2020 0 (3) e363-e365 - Dural Venous Sinus Thrombosis and Papilledema Related to JAK2 Mutation: A Case Series.
Donaldson Laura, et al. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2021 0 1-7 - Ocular manifestations in Chinese adult patients with NLRP3-associated autoinflammatory disease.
Meng Tianli, et al. Scientific reports 2021 6 (1) 11904 - Artificial Intelligence to Detect Papilledema from Ocular Fundus Photographs.
Milea Dan et al. The New England journal of medicine 2020 Apr (18) 1687-1695 - AI for the Eye — Automated Assistance for Clinicians Screening for Papilledema
I Kohane, NEJM, April 14, 2020 - Hereditary thrombophilia in cerebral venous thrombosis: a study from India.
Pai Navin, et al. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2013 7 (5) 540-3 - [A clinical study of Leber hereditary optic neuropathy].
Wei Qi-Ping, et al. [Zhonghua yan ke za zhi] Chinese journal of ophthalmology 2012 12 (12) 1065-8 - Papilledema
From NCATS Genetic and Rare Diseases Information Center
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
- Page last updated:Apr 25, 2024
- Content source: