User Posts: Dr. Gelareh Abedi, MD - Ophthalmologist
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Anophthalmia
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Anophthalmia is a rare congenital condition characterized by the complete absence of one or both eyes (the globe) and all associated ocular tissues within the ...

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Anomalous Retinal Correspondence (ARC)
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Anomalous Retinal Correspondence (ARC) is a sensory adaptation in which the brain learns to fuse images from two misaligned eyes by remapping the extra-foveal ...

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Ankyloblepharon
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Ankyloblepharon is a medical condition characterized by the adhesion or fusion of the edges of the upper eyelid with those of the lower eyelid, either ...

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Anisometropic Amblyopia
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Anisometropic amblyopia, often called “lazy eye” caused by unequal refractive error, is a vision development disorder in which the brain favors one eye over ...

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Aniseikonia
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Aniseikonia is a binocular vision disorder in which the images perceived by each eye differ in size or shape. In simple terms, an object viewed by one eye ...

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Aniridic Fibrosis Syndrome
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Aniridic Fibrosis Syndrome is a rare, sight-threatening complication that arises in patients with congenital aniridia—an eye condition marked by partial or ...

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Aniridia
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Aniridia is a rare eye condition characterized by the complete or near-complete absence of the iris, the colored muscular ring that regulates how much light ...

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Angle Recession Glaucoma (ARG)
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Angle Recession Glaucoma (ARG) is a form of secondary open-angle glaucoma that develops after blunt injury to the eye. In this condition, trauma causes a ...

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Angiolymphoid Hyperplasia with Eosinophilia
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Angiolymphoid hyperplasia with eosinophilia (ALHE), also called epithelioid hemangioma, is a rare, benign vascular proliferation characterized by the growth of ...

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Angioid Streaks
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Angioid streaks are irregular fissures or crack-like breaks in Bruch’s membrane, a thin, elastic layer that lies between the retina and the choroid. These ...

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Angelman Syndrome
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Angelman syndrome is a rare neuro-genetic disorder caused by the loss of function of the maternal UBE3A gene on chromosome 15. In most healthy individuals, ...

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Amiodarone-Associated Optic Neuropathy (AAON)
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Amiodarone‐associated optic neuropathy (AAON) is a rare, drug‐induced damage to the optic nerve that occurs in patients receiving amiodarone for cardiac ...

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Amblyopia
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Amblyopia, commonly known as “lazy eye,” is a vision development disorder in which an eye fails to achieve normal visual acuity—sharpness—even with ...

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Transient Vision Loss
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Transient vision loss (TVL) refers to a temporary loss of vision, either partial or complete, in one or both eyes, lasting from a few seconds up to 24 hours. ...

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Amaurosis Fugax
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Amaurosis fugax is a transient, painless loss of vision in one or both eyes, typically lasting from seconds to minutes before returning to normal. It occurs ...

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Amantadine-Induced Corneal Edema
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Amantadine-induced corneal edema is a rare but recognized toxic reaction in which the drug amantadine damages the inner cell layer of the cornea (the ...

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Alpha-Gal Syndrome
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Alpha-Gal Syndrome (AGS) is a potentially life-threatening, IgE-mediated allergic condition in which the body reacts to the carbohydrate ...

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Alice in Wonderland Syndrome (AIWS)
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Alice in Wonderland Syndrome (AIWS) is a rare neurological condition that makes a person’s perceptions of their own body or the world around them feel ...

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Alexia without Agraphia (Pure Alexia)
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Alexia without agraphia, often called pure alexia or word blindness, is a rare neurological condition in which a person loses the ability to read printed text ...

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Alagille Syndrome
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Alagille syndrome is a rare genetic disorder that primarily affects the liver and heart, but can also involve the eyes, skeleton, kidneys, and blood vessels. ...

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Akinetopsia
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Akinetopsia, often called “motion blindness,” is a rare neurological disorder in which a person cannot perceive motion in their visual field. Instead of seeing ...

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Aicardi Syndrome
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Aicardi syndrome is a rare neurodevelopmental disorder primarily affecting females, characterized by the absence of the corpus callosum, distinctive retinal ...

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Ageism in Neuro-Ophthalmology
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Ageism in Neuro-Ophthalmology refers to the stereotypes, prejudices, and discriminatory practices that affect older (and sometimes younger) patients when they ...

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Age-Related Macular Degeneration (AMD)
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Age-Related Macular Degeneration (AMD) is a chronic eye condition that gradually destroys sharp, central vision, essential for activities like reading, ...

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Advancing Wavelike Epitheliopathy
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Advancing wavelike epitheliopathy (AWE) is a chronic or recurrent disorder of the corneal epithelium characterized by well-demarcated, wavelike plaques of ...

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Adult-Onset Asthma with Periocular Xanthogranuloma (AAPOX)
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Adult-Onset Asthma with Periocular Xanthogranuloma (AAPOX) is a rare, multisystem inflammatory disorder characterized by the combination of new-onset asthma in ...

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Adie Pupil
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Adie pupil—also called Adie’s tonic pupil—is a neurological condition in which one or both pupils are abnormally dilated (larger than normal) and react poorly ...

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Adenoid Cystic Carcinoma of the Lacrimal Gland
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Adenoid cystic carcinoma of the lacrimal gland is a rare but aggressive malignant tumor that arises from the secretory epithelial cells of the tear-producing ...

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Adaptive Optics
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Adaptive optics (AO) is an advanced technology used to improve the clarity and resolution of images taken through systems that suffer from optical distortions. ...

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ADAMTSL4-Related Eye Disorders
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ADAMTSL4-related eye disorders are rare autosomal recessive conditions characterized by lens displacement (ectopia lentis), often with pupillary displacement ...

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Acute Zonal Occult Outer Retinopathy (AZOOR)
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Acute Zonal Occult Outer Retinopathy (AZOOR) is a rare retinal disease first described by J. Donald Gass in 1992. It is classified within the “white dot ...

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Krill’s Disease
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Krill’s disease, commonly known as Acute retinal pigment epitheliitis (ARPE), is a rare, idiopathic, self-limiting inflammatory disorder of the macula first ...

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Acute Retinal Pigment Epitheliitis
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Acute Retinal Pigment Epitheliitis (ARPE), sometimes called Krill’s disease, is a rare, self‐limiting inflammation of the retinal pigment epithelium (RPE). The ...

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Acute Retinal Pigment Epitheliitis (ARPE)
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Acute Retinal Pigment Epitheliitis (ARPE), also known as Krill’s disease, is a rare, idiopathic, self-limiting inflammatory disorder affecting the macula of ...

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Acute Retinal Necrosis
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Acute retinal necrosis (ARN) is a rare but serious inflammatory condition of the eye characterized by rapid, full-thickness death of retinal tissue, typically ...

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Acute Posterior Multifocal Placoid Pigment Epitheliopathy (APMPPE)
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Acute Posterior Multifocal Placoid Pigment Epitheliopathy (APMPPE) is a rare, acute, inflammatory chorioretinal disorder classified among the “white dot ...

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Acute Macular Neuroretinopathy (AMN)
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Acute Macular Neuroretinopathy (AMN) is a rare eye condition that affects the macula, the central part of the retina responsible for sharp, detailed vision. It ...

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Acute Idiopathic Blind Spot Enlargement (AIBSE) Syndrome
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Acute Idiopathic Blind Spot Enlargement (AIBSE) Syndrome is a rare, self-limiting disorder of the outer retina first described by Fletcher and Imes in 1988. It ...

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Acute Exudative Polymorphous Vitelliform Maculopathy (AEPVM)
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AEPVM is an uncommon retinal disorder first delineated by Gass et al. in 1988. It presents bilaterally with multiple, yellow-white lesions at the level of the ...

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Types of Acute Disseminated Encephalomyelitis
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Acute disseminated encephalomyelitis (ADEM) is a rare, autoimmune, demyelinating disorder of the central nervous system characterized by a sudden, widespread ...

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Acute Corneal Hydrops
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Acute corneal hydrops is a sudden, sight-threatening complication of corneal ectatic disorders—most commonly keratoconus—characterized by an abrupt rupture in ...

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Acute Anterior Uveitis
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Acute anterior uveitis (AAU) is a sudden inflammation of the front part of the uvea, specifically the iris (colored ring of the eye) and the ciliary body ...

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Actinic Keratosis
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Actinic keratosis (AK) is a common precancerous skin lesion characterized by rough, scaly patches that develop on sun-exposed areas of skin. These lesions ...

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Acquired Supranuclear Ocular Motor Paresis (ASOMP)
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Acquired supranuclear ocular motor paresis (ASOMP) is a neurological condition characterized by a selective inability to initiate or control voluntary eye ...

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Acquired Retinal Macroaneurysm (RAM)
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An acquired retinal macroaneurysm (RAM) is a focal, abnormal dilation of a retinal arteriole wall, typically between 100 and 250 μm in diameter, occurring ...

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Acquired Oculomotor Nerve Palsy
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Acquired oculomotor nerve palsy is a non-congenital condition in which the third cranial nerve (oculomotor nerve) becomes damaged after birth, leading to ...

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Acquired Ectropion Uveae
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Acquired ectropion uveae (AEU) is a condition in which the pigmented posterior layer of the iris—normally hidden on the back surface—becomes adherent to and ...

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Achromatopsia
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Achromatopsia is a rare, inherited vision disorder that causes a complete or partial inability to see color. People with achromatopsia rely almost entirely on ...

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Accommodative Esotropia
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Accommodative esotropia is a common form of childhood strabismus in which one or both eyes turn inward (esodeviation) because of excessive focusing ...

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Acanthamoeba Keratitis
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Acanthamoeba keratitis is a rare but potentially sight-threatening corneal infection caused by the free-living amoeba Acanthamoeba, which is found ubiquitously ...

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Ablepharon-Macrostomia Syndrome
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Ablepharon-Macrostomia Syndrome (AMS) is an extremely rare, autosomal dominant genetic disorder characterized principally by absent or underdeveloped eyelids ...

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Types of Abducens Nerve Palsy
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Abducens nerve palsy, also called sixth cranial nerve palsy, is a condition where the sixth cranial nerve (the abducens nerve) stops sending proper signals to ...

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