Talk:New Article Requests
Before You Submit a Proposal
- EVALUATION CRITERIA: Review these to be sure your proposal is eligible.
- EXISTING ARTICLES: Review these to see if your proposed topic is already included or could be inlcuded in an existing EyeWiki article. You can do this by performing a thorough search using various related key terms.
- If you find a pre-existing stand-alone article that addresses your topic or an article that includes your topic please edit the article to include your own input. You will be automatically recognized as a contributor to that article.
- Of those proposals that are not accepted, 85% are rejected because the topic is already covered or could be covered in an existing EyeWiki article.
- PROPOSALS PREVIOUSLY SUBMITTED: Review these and please do not resubmit these topics.
Instructions
- IMPORTANT: Review the section above "Before You Submit a Proposal"
- Click the "Add topic" link to create a new proposal on this page
- Then add the relevant list items as shown
- Title: Enter this in the Subject field
- Summary: Please provide some details about what will be covered and why you think the article would benefit EyeWiki. Do not submit a complete article.
- Section: Indicate what subspecialty section the article should be added to. You may indicate up to 2 sections.
- Submitted by: Name of the ophthalmologist submitting the proposal. Sign and date your request by entering 4 tilde ~ characters only. This will automatically add your username, a time stamp and a link to your profile. You will see this after you save the page.
- SAMPLE: Rayna.Ungersma.AAO (talk) 10:01, April 30, 2024 (PDT)
- Click: SAVE at the bottom of the page
Sample Proposal
Biosimilars in Ophthalmology
Summary: Patents for original biologics used to treat nAMD and DME are approaching expiration. Numerous companies are striving to replicate these biologics as biosimilars, which are drugs that mimic the effects of the original biologic, but do not have the same active ingredients. This article will summarize the current literature about biosimilars and their safety, efficacy, and quality and provide an in-depth review of approved biosimilars as well as those that are in development. This article will provide EyeWiki readers with information about numerous alternatives for treatment nAMD and DME.
Section: Retina/Vitreous
Submitted by: Rayna.Ungersma.AAO (talk) 15:04, May 1, 2024 (PDT)
Goldmann-Favre Syndrome
Summary: Goldmann-Favre Syndrome (GFS) is a rare autosomal recessive vitreoretinopathy caused by mutations in the NR2E3 gene, which affects photoreceptor development and function. It is characterized by night blindness (nyctalopia), progressive visual impairment, and peripheral retinal degeneration due to abnormal photoreceptor differentiation. Goldmann-Favre Syndrome remains underrecognized due to its rarity, yet it has significant implications for differential diagnosis and genetic counseling. This article aims to provide an accessible, evidence-based review for ophthalmologists, retina specialists, and researchers seeking to better understand this condition.
Section: Retina/Vitreous
Submitted by: Hashem.AbuSerhan (talk) 07:56, February 15, 2025 (PST)
Retinitis Punctata Albescens
Summary: Retinitis Punctata Albescens (RPA) is a rare autosomal recessive retinal dystrophy that belongs to the spectrum of retinitis pigmentosa (RP). It is characterized by numerous small white retinal dots, mainly in the midperipheral and peripheral retina, along with progressive night blindness (nyctalopia) and visual field constriction.
Given the rarity of this inherited vitreoretinopathy and its implications for clinical practice, I believe a well-structured, up-to-date article on this topic would be a valuable addition to the EyeWiki knowledge base.
Section: Retina/Vitreous
Submitted by: Hashem.AbuSerhan (talk) 03:20, February 16, 2025 (PST)
Snowflake Vitreoretinal Degeneration
Summary: Snowflake Vitreoretinal Degeneration (SVD) is a rare autosomal dominant inherited retinal disorder characterized by progressive vitreous degeneration, peripheral retinal atrophy, and retinal crystalline deposits resembling snowflakes. It can lead to progressive vision loss and an increased risk of retinal detachment. Snowflake Vitreoretinal Degeneration is a poorly understood yet clinically relevant disease. Many ophthalmologists may not recognize its unique fundus findings and progression, leading to misdiagnosis or delayed intervention. Since SVD significantly increases the risk of retinal detachment, awareness among ophthalmologists and retina specialists is crucial. A comprehensive article on EyeWiki would help improve early recognition and appropriate management strategies.
Section: Retina/Vitreous
Submitted by: Hashem.AbuSerhan (talk) 03:24, February 16, 2025 (PST)
Incontinentia Pigmenti (IP) – Ocular Manifestations
Summary: Incontinentia Pigmenti (IP) is a rare X-linked dominant disorder affecting ectodermal tissues, including the skin, central nervous system, and eyes. It primarily occurs in females, as male fetuses with IP mutations often do not survive. Ocular involvement in IP can be vision-threatening due to retinal vascular abnormalities leading to retinal detachment. Although IP is widely recognized for its dermatologic findings, its ocular manifestations are less well-known, despite their severe impact on vision. EyeWiki would provide a dedicated ophthalmology-focused resource for this disease. Many cases of IP-associated retinal detachment go undetected due to delayed screening. This article would highlight the importance of early fundus examinations in affected infants to prevent vision loss. Since IP is a systemic disorder, ophthalmologists, pediatricians, and neonatologists should be aware of its ocular risks. A comprehensive EyeWiki article would bridge the knowledge gap between specialties. IP shares similarities with ROP, familial exudative vitreoretinopathy (FEVR), and Coats' disease. An EyeWiki article would help clinicians differentiate these conditions and tailor management appropriately.
Section: Retina/Vitreous
Submitted by: Hashem.AbuSerhan (talk) 03:28, February 16, 2025 (PST)
Frontalis Muscle Advancement
- Summary: The proposed article will provide a comprehensive overview of frontalis muscle advancement, a crucial surgical technique for managing blepharoptosis with poor or absent levator function. The article will cover essential aspects including surgical anatomy, patient selection criteria, detailed surgical technique, postoperative management, and potential complications. This topic warrants coverage on Eyewiki, as it represents an important alternative to traditional frontalis slings. Currently, there does not appear to be an article or description of this surgery. The article will serve as a valuable resource for residents, fellows, and practicing surgeons.
- Section: Oculoplastics/Orbit
- Submitted by: Anne.Barmettler (talk) 08:27, February 20, 2025 (PST)
Hereditary angioplasty with nephropathy, aneurysms, and muscle cramps (HANAC)
Hereditary angioplasty with nephropathy, aneurysms, and muscle cramps (HANAC) is a hereditary disorder of autosomal dominance involving a mutation of the COL4A1 gene, which causes issues in basement membrane structural integrity of blood vessels systemically - including the retinal vessels. This article will review etiology, signs and symptoms of HANAC, differentiating factors between HANAC and hypertensive retinopathy, renal manifestations and management, the importance of primary prevention of stroke.
Section: Retina
Submitted by: Sruti.Rachapudi (talk) 10:13, February 21, 2025 (PST)