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Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHADD)-Associated Ocular Pathology—A Narrative Review

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) is an extremely rare autosomal recessive disorder, with only a few hundred affected individuals worldwide. Since its initial recognition in the 1980s, only a limited number of studies have described its ocular manifestations. The aim of...

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Principais autores: Magdalena Hubert, Maciej Gawęcki
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI AG 2026-01-01
coleção:Diagnostics
Assuntos:
long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
chorioretinopathy
macular neovascularization
myopia
Acesso em linha:https://www.mdpi.com/2075-4418/16/2/295
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