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. Author manuscript; available in PMC: 2024 Apr 12.
Published in final edited form as: Ophthalmic Genet. 2024 Jan 30;45(2):140–146. doi: 10.1080/13816810.2024.2303682

Table 1.

Clinical staging based on multimodality ophthalmological findings of patients with LCHADD chorioretinopathy.

Fundus
OCT
Stage Posterior pole Periphery FfERG Wide field FAF Retinal findings Choroidal findings

1 normal normal normal normal normal
2 A pigmentary deposition in the macular area Normal speckled hypo/hyperautofluorescence mostly within posterior pole and vascular arcades normal to thickening of RPE-Bruch complex in macular, mild attenuation of EZ/RPE can be observed normal
B more prominent pigmentary deposition spreading beyond the vascular arcades into the midperiphery mildly to moderately decreased ffERG speckled hypoautofluorescence beyond vascular arcades to the midperiphery normal to thickening of RPE-Bruch complex in central fovea, mild attenuation of EZ/RPE can be observed normal
3 A partial chorioretinal atrophy, relative sparing of the central macula pigmentary deposition beyond arcades and to periphery mild to moderately decreased ffERG Progressive enlargement of hypo autofluorescence from RPE loss (usually multiple well-demarcated nummular lesions) in macular area out towards the mid-periphery,
with a meshwork of residual RPE hyperautofluorescence sparing
Progressive outer retina (EZ, RPE-Bruch membrane, ONL) attenuation, outer retinal tubulation choroidal thickness normal or mild thinning
B moderate to severely decreased ffERG enlargement areas of hypoautofluorescence toward mid-periphery with a meshwork of residual RPE hyperautofluorescence sparing progressive outer retinal atrophy, outer retinal tubulation progressive choroidal atrophy sparing central fovea (abrupt transition zones)
4 extensive atrophy of the posterior pole, totally loss central island in some cases, posterior staphyloma pigmentary changes and progressive atrophy toward periphery moderate to severely decreased ffERG
to non-recordable
enlargement area of hypoautofluorescence with some degree of intact peripheral retina extensive outer retinal atrophy, outer retinal tubulation extensive choroidal atrophy sparing central fovea in most cases
*

concurrent ocular findings which can be observed at Stage 2 and higher; CNV: choroidal neovascularization, ERM: epiretinal membrane, CME: cystoid macular edema.

LCHADD: long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency, ffERG: full-field electroretinography, FAF: fundus autofluorescence, OCT: optical coherence tomography, RPE: retinal pigment epithelium, EZ: ellipsoid zone, ONL: outer nuclear layer.