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Medical condition
Amaurosis fugax (Ancient Greek: ἀμαύρωσις, amaurosis meaning 'darkening', 'dark', or 'obscure', Latin: fugax meaning 'fleeting') is a painless temporary
Amaurosis_fugax
Rare inherited eye disease
Leber congenital amaurosis (LCA) is a rare inherited eye disease that appears at birth or in the first few months of life. It affects about 1 in 40,000
Leber_congenital_amaurosis
Loss of vision
Amaurosis (Greek meaning darkening, dark, or obscure) is vision loss or weakness that occurs without an apparent lesion affecting the eye. It may result
Amaurosis
Decreased ability to see
of inherited blindness, known as Leber's congenital amaurosis or LCA. Leber's Congenital Amaurosis damages the light receptors in the retina and usually
Visual_impairment
Medical condition
however human clinical trials for both choroideremia and Leber's congenital amaurosis (LCA) have produced somewhat promising results. Clinical trials of gene
Choroideremia
Gradual retinal degeneration leading to progressive sight loss
therapy that is commercially available to RP patients with Leber congenital amaurosis type 2. It replaces the miscoded RPE65 protein that is produced within
Retinitis_pigmentosa
Part of the eye
already reported positive results using rAAV to treat Leber's congenital amaurosis, showing that the therapy was both safe and effective. There were no serious
Retina
Medical condition
symptoms. "Orphanet: Amaurosis hypertrichosis syndrome". www.orpha.net. Retrieved 2022-06-13. "OMIM Entry - 204110 - Amaurosis Congenita, Cone-Rod Type
Amaurosis congenita, cone-rod type, with congenital hypertrichosis
Amaurosis_congenita,_cone-rod_type,_with_congenital_hypertrichosis
Gene therapy medication
therapy medication for the treatment of Leber congenital amaurosis. Leber's congenital amaurosis, or biallelic RPE65-mediated inherited retinal disease
Voretigene_neparvovec
Health condition negatively affecting the eye
transmission of the visual image to the brain (H53.0) Leber's congenital amaurosis – genetic disorder; appears at birth, characterised by sluggish or no
Eye_disease
Dysfunction of eye movement
cataract Bilateral optic nerve hypoplasia Idiopathic Leber's congenital amaurosis Optic nerve or macular disease Persistent tunica vasculosa lentis Rod
Nystagmus
Blindness present at birth
these include: Microphthalmia Anophthalmia Coloboma Leber's congenital amaurosis (LCA) is a collection of inherited, degenerative eye disorders that can
Congenital_blindness
Medical technology
technique. These include treatment of retinal diseases Leber's congenital amaurosis and choroideremia, X-linked SCID, ADA-SCID, adrenoleukodystrophy, chronic
Gene_therapy
Protein-coding gene in humans
Mutations in the RPE65 gene have been associated with Leber's congenital amaurosis type 2 (LCA2) and retinitis pigmentosa (RP). RPE65 has been isolated from
RPE65
Group of eye diseases related to poor retinal and nerve perfusion
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Glaucoma
Decreased ability to see color or color differences
blindness, including achromatopsia, cone dystrophy, Leber's congenital amaurosis and retinitis pigmentosa. These can be congenital or commence in childhood
Color_blindness
Eyes not aligning when looking at something
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Strabismus
Type of eye defect
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Astigmatism
Species of virus
Phase 2 trials for a number of diseases, including Leber's congenital amaurosis, hemophilia, congestive heart failure, spinal muscular atrophy, lipoprotein
Adeno-associated_virus
Inflammation of the uvea of the eye
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Uveitis
Clouding of the lens inside the eye, causing poor vision
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Cataract
Inability to focus on distant objects
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Myopia
Medical condition of the eye
but later studies suggest such loss is a relatively rare side effect. Amaurosis fugax Entoptic phenomenon Scintillating scotoma Grosberg BM, Solomon S
Retinal_migraine
Failure of the brain to process input from one eye
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Amblyopia
Physiological process
cells for this conversion. A possible mechanism for Leber's congenital amaurosis has been proposed as the deficiency of RPE65. Without the RPE65 protein
Visual_cycle
Inflammation of the eye
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Conjunctivitis
Abnormal intolerance to visual perception of light
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Photophobia
Vision loss due to damage to the macula of the eye
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Macular_degeneration
Difference in coloration, usually of the iris but also of hair or skin
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Heterochromia
Deposits within the eye's vitreous humour
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Floater
intercourse (N94.1) pelvic pain vaginal discharge Ocular amaurosis fugax (G45.3) and amaurosis blurred vision Dalrymple's sign double vision (H53.2) exophthalmos
List_of_medical_symptoms
Medical condition
ophthalmologist. The diagnosis may be suspected in people with visual loss or amaurosis fugax. AAION occurs in elderly and late middle-aged people. Certain blood
Arteritic anterior ischemic optic neuropathy
Arteritic_anterior_ischemic_optic_neuropathy
Absence of the iris, usually involving both eyes
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Aniridia
Presence of abundant hair between the eyebrows
syndrome 1 Acromegaloid facial appearance syndrome Acromesomelic dysplasia 4 Amaurosis-hypertrichosis syndrome Arrhinia with choanal atresia and microphthalmia
Unibrow
Medical university in Portland, Oregon, United States
procedure is intended to reverse a genetic mutation causing Leber congenital amaurosis, a form of inherited blindness. OHSU explored an integration with Legacy
Oregon Health and Science University
Oregon_Health_and_Science_University
Excessive dilation of the pupil
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Mydriasis
Inflammation of the eyelid
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Blepharitis
Swelling of the eyelid due to infection of an oil gland
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Stye
Form of strabismus in which the eyes turn inward
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Esotropia
Loss of vision without any organic cause
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Functional_visual_loss
Surname list
ophthalmologist who first described the diseases now known as Leber's congenital amaurosis and Leber's hereditary optic neuropathy Titus Leber, Austrian film director
Leber
Medical condition
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Congenital_fourth_nerve_palsy
Protein-coding gene in the species Homo sapiens
in Philadelphia, where researchers are hopeful that Leber Congenital Amaurosis will one day be cured. This gene encodes a protein with 13 putative coiled-coil
CEP290
Excessive constriction of the pupil
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Miosis
Topics referred to by the same term
Temporary blindness, a type of non-permanent vision loss, may refer to: Amaurosis fugax, or fleeting blindness Conversion disorder, formerly called hysterical
Temporary_blindness
Experimental medical treatment
FDA was Voretigene neparvovec in 2017, which treats Leber's congenital amaurosis, a genetic disorder that can lead to blindness. These treatments also
Gene therapy for color blindness
Gene_therapy_for_color_blindness
Most common genetic condition leading to color blindness
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Congenital red–green color blindness
Congenital_red–green_color_blindness
Drooping of the upper eyelid over the eye
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Ptosis_(eyelid)
disease, familial Amaurosis Amaurosis congenita of Leber Amaurosis congenita of Leber, type 1 Amaurosis congenita of Leber, type 2 Amaurosis hypertrichosis
List_of_diseases_(A)
Medical condition
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Fuchs'_dystrophy
Medical condition involving the eye
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Keratoconus
Visual aura associated with migraine
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Scintillating_scotoma
Lack of blood flow within the eye
symptoms secondary to severe, chronic arterial hypoperfusion to the eye. Amaurosis fugax is a form of acute vision loss caused by reduced blood flow to the
Ocular_ischemic_syndrome
Surgical procedure
Symptomatic people have had either a stroke or transient ischemic attack or amaurosis fugax. In symptomatic patients with a 70–99% stenosis, for every six people
Carotid_endarterectomy
Medical condition
lupus, or a family history of cerebrovascular or cardiovascular issues. Amaurosis fugax Branch retinal artery occlusion Branch retinal vein occlusion Central
Central retinal artery occlusion
Central_retinal_artery_occlusion
Protein-coding gene in the species Homo sapiens
protein is a member of FKBP prolyl isomerase family. Leber congenital amaurosis (LCA) accounts for at least 5% of all inherited retinal disease and is
AIPL1
Topics referred to by the same term
voretigene neparvovec, a gene therapy for the treatment of Leber's congenital amaurosis Sanctuary lamp or eternal light Lux perpetua (disambiguation), synonymous
Lux_Aeterna
Minor form of stroke
focal neurologic deficits, which can include, but are not limited to: Amaurosis fugax (painless, temporary loss of vision) One-sided facial droop One-sided
Transient_ischemic_attack
Inflammatory swelling of the eyelid due to meibomian gland blockage
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Chalazion
Gene editing method
CRISPR treatment for LCA10 (the most common variant of Leber congenital amaurosis which is the leading cause of inherited childhood blindness) modifies
CRISPR_gene_editing
Organism altered by genetic engineering
disorders such as severe combined immunodeficiency and Leber's congenital amaurosis. Many objections have been raised over the development of GMOs, particularly
Genetically_modified_organism
Eye condition caused by ultraviolet radiation
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Photokeratitis
Bulging of the eye anteriorly out of the orbit
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Exophthalmos
Fictional character
Angela and Hodgins find out they are both carriers of Leber's Congenital Amaurosis, giving their baby a 25 percent chance of blindness. This is a huge devastation
Jack_Hodgins_(Bones)
Medical condition
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Retinitis
American baseball player (born 1975)
Lee's three-year-old daughter Jada was diagnosed with Leber's congenital amaurosis, a rare genetic disease resulting in loss of vision. Lee and Boston Celtics
Derrek_Lee
Disease that damages the myelin sheaths around nerves
1948. His symptoms began at age 28 with a sudden transient visual loss (amaurosis fugax) after the funeral of a friend. During his disease, he developed
Multiple_sclerosis
Medical condition
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Primary_congenital_glaucoma
Medical condition
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Oculogyric_crisis
Clouding of the transparent cornea of the eye
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Corneal_dystrophy
Blockage of the central retinal vein in the eye
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Central retinal vein occlusion
Central_retinal_vein_occlusion
Dry eye
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Xerophthalmia
Unequal size of the eyes' pupils
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Anisocoria
Double vision
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Diplopia
Condition making it difficult or impossible to see in relatively low light
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Nyctalopia
Discovery-phase pharmaceutical company
trial using CRISPR gene editing techniques to treat Leber congenital amaurosis type 10 (LCA10), a rare genetic illness that causes blindness. On 30 November
Editas_Medicine
Medical condition
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Iridodialysis
Medical condition
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Graves'_ophthalmopathy
Protein-coding gene in the species Homo sapiens
RPGR-interacting domain (RID). Defects in the gene result in the Leber congenital amaurosis (LCA) syndrome and in the eye disease glaucoma. RPGRIP1 has been shown
RPGRIP1
Type of eye infection
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Toxoplasmic_chorioretinitis
American artist
they had to pick the two which were most alike. The seventh installment, Amaurosis, focuses on blind guitarist Nguyen Duc Dat through his life as an American
Tran_T._Kim-Trang
Medical condition
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Achromatopsia
American singer-songwriter
has only a two-percent field of vision, both due to Leber's congenital amaurosis. MacIntyre was born in Redondo Beach, California to Douglas R. and Carole
Scott_MacIntyre
Inability to turn out the eye due to dysfunction of the abducens nerve
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Sixth_nerve_palsy
Swelling of the conjunctiva
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Chemosis
Insufficient bloodflow to the brain
unilateral weakness, speech disturbances, or visual loss in one eye (amaurosis fugax).Posterior circulation ischemia, involving the vertebrobasilar arteries
Brain_ischemia
Artery of the head
cherry-red spot is typically absent and the vision is usually worse. Amaurosis fugax is a temporary loss of vision that occurs in two conditions which
Ophthalmic_artery
Condition of misalignment of the eyes
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Hypertropia
Medical condition
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Exposure_keratopathy
Eye condition in which light is focused behind instead of on the retina
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Farsightedness
Rare congenital disease characterized by external gaze palsy
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Duane_syndrome
Reduced ability of the eyes to turn inward when focusing
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Convergence_insufficiency
Medical condition
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Arcus_senilis
Disease found in young children
found as uveitis, iridocyclitis, conjunctival hemorrhage, optic neuritis, amaurosis, and ocular artery obstruction. It can also be found as necrotizing vasculitis
Kawasaki_disease
Medical condition associated with aging of the eye
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Presbyopia
Medical condition
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Herpes_simplex_keratitis
Medical condition
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Trochleitis
Medical condition
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Macular_edema
Visual perception disorder
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Bálint's_syndrome
Medical condition
membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary
Vogt–Koyanagi–Harada_disease
AMAUROSIS
AMAUROSIS
AMAUROSIS
AMAUROSIS
Boy/Male
Indian, Punjabi, Sikh
Glow of the Lord
Boy/Male
Sikh
Humble, Meek, Obedient
Male
English
Anglicized form of Irish Gaelic Réamann, REDMOND means "wise protector."
Girl/Female
Indian, Sikh
Filled with Fragrance
Female
Arthurian
, noble cheer, or, noble maiden.
Boy/Male
Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Tamil, Telugu
The One who has Learnt All Vedas
Girl/Female
Hindu, Indian, Traditional
Nourishing
Girl/Female
Australian, Danish, Irish
Temptress; Hardworking
Male
Native American
Native American Winnebago name NAWKAW means "wood."
Boy/Male
Gaelic
Son of Arthur.
AMAUROSIS
AMAUROSIS
AMAUROSIS
AMAUROSIS
AMAUROSIS
n.
A loss or decay of sight, from loss of power in the optic nerve, without any perceptible external change in the eye; -- called also gutta serena, the "drop serene" of Milton.
a.
Affected with amaurosis; having the characteristics of amaurosis.
n.
Weakness of sight, without and opacity of the cornea, or of the interior of the eye; the first degree of amaurosis.
n.
A species of blindness in horses in which the eye is bright and the pupil dilated; a sort of amaurosis.