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Rzadka choroba narządu wzroku, która zwykle charakteryzuje się postępującą utratą widzenia centralnego wskutek obecności nieregularnych biało-żółtych punktowych zmian w obrębie i wokół plamki żółtej oraz zanikowych zmian w centralnym obszarze plamki o charakterze tzw. „bitego brązu”.
1 gru 2014 · Fluorescein angiography (FA), fundus autofluorescence (FAF), and spectral-domain optical coherence tomography (SD-OCT) can help diagnose and characterize Stargardt disease. The hallmark finding on imaging of Stargardt disease is a “dark choroid” on FA . This sign, in which the retinal circulation appears to be highlighted against a ...
Stargardt disease (STGD1) is caused by bi-allelic ABCA4 gene variants (i.e., autosomal recessive). Importantly, the exact genotype (i.e., combinations of both ABCA4 variants along with the presence of additional genetic modifiers [ 5 ] ) is highly prognostic for the age of onset and disease progression.
ICD 10 code for Unspecified hereditary retinal dystrophy. Get free rules, notes, crosswalks, synonyms, history for ICD-10 code H35.50.
8 sty 2024 · Stargardt disease type 1 (STGD1) is the most common cause of juvenile macular dystrophy. [1] German ophthalmologist Karl Stargardt first described the condition in 1909 in seven patients of two families who presented with macular dystrophy surrounded by yellow-white pisciform flecks.
Diagnostic evaluation of Stargardt disease is based on family history, visual acuity, fundus examination, visual field testing, fluorescein angiography, fundus autofluorescence (FAF), electroretinography (ERG) and optical-coherence tomography (OCT).
The clinical diagnosis is based on ophthalmological examinations consisting of visual acuity and visual field testing, ophthalmoscopy, electroretinography (ERG), fluorescein angiography (FA), fundus autofluorescence (FAF), and optical coherence tomography (OCT), revealing macular anomalies (progressive atrophy often in a 'beaten bronze pattern ...
