American journal of ophthalmology۲۰۲۶نمایه شده در PubMed
Emma Sieg, Johannes Birtel, Jan Wildner, Nikolaos Gkalapis, Martin S Spitzer, Mona Lindschau, Nicole Muschol, Yevgeniya Atiskova
چکیده
Mucopolysaccharidosis type III (MPS III, Sanfilippo syndrome) is a group of rare, hereditary, autosomal recessive, lysosomal storage disorders characterized by neurocognitive decline and early mortality. Pronounced visual impairment is frequent and retinal disease is more common in MPS III than in…
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DOI: 10.1016/j.ajo.2026.03.005