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  1. 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 ( Fig. 2 ).

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  2. 8 sty 2024 · Identify the genetics related to Stargardt disease and describe the various clinical features and differential diagnosis of this condition. Interpret the various imaging modalities used to diagnose and assess Stargardt disease.

  3. 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).

  4. 13 paź 2022 · How is Stargardt disease diagnosed? Your provider will take a complete medical history and do a physical examination. They will perform: A dilated eye exam. Optical coherence tomography (OCT). Electroretinography (ERG) to test your retina’s responses in different types of light.

  5. 22 paź 2024 · Diagnosis of Stargardt disease is through a dilated eye exam to observe yellowish deposits in the macula known as lipofuscin. Other tests may include fluorescein angiography, electroretinography (ERG), visual field testing, color vision testing, fundus photography OCT, and genetic testing.

  6. 3 wrz 2024 · Stargardt disease is an eye disease that causes vision loss in children and young adults. It is an inherited disease, meaning it is passed on to children from their parents. Stargardt disease is often called juvenile macular dystrophy (sometimes called juvenile macular degeneration).

  7. 29 wrz 2021 · Stargardt disease is a rare genetic eye disease that causes vision loss in childhood or adolescence. Learn how an eye doctor can diagnose it with a dilated eye exam, photos or scans of the retina, and genetic testing.

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