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. 2015 Apr 2;2015:940864. doi: 10.1155/2015/940864

Table 1.

Clinical features of STGD patients with ABCA4 mutations.

Family ID Age/sex BCVA Refraction Fundus FAF SD-OCT Full field ERG
RE LE RE LE
SG-01_II:1 27/M 6/60, N8 6/36, N8 −2.5 DS −2.75 DS Macular atrophy, no flecks Hypo-AF surrounded by ring of hyper-AF IS/OS loss Normal

SG-02_II:1 31/M 6/60, N34 4/60, N36 0 0 Macular atrophy, macular flecks Hypo-AF surrounded by hyper- and hypo-AF flecks IS/OS loss Normal

SG-03_II:1 22/M 6/60, N18 6/45, N18 −1.25 DS/
−1.00 DC 90°
−1.50 DS/
−0.50 DC 20°
Macular atrophy, extensive flecks Hypo-AF surrounded by hyper- and hypo-AF flecks IS/OS loss Rod-cone dysfunction

SG-04_II:1 26/M 6/38, N12 6/38, N12 −1.00 DS/
−0.5 DC 70°
−1.50 DS Macular atrophy, no flecks NA IS/OS loss Normal

SG-05_V:1 16/F 6/60, N12 6/38, N12 +0.5 DS/
−0.75 DC 5°
+0.5 DS/
−0.75 DC 170°
Macular atrophy, temporal pallor of optic discs Hypo-AF surrounded by hyper-AF flecks IS/OS loss Cone-rod dysfunction

BCVA: best corrected visual acuity, RE: right eye, LE: left eye, BE: both eyes, IOP: intraocular pressure, PR: photoreceptors, AF: autofluorescent, SD-OCT: spectral domain optical coherence tomography, FAF: fundus autofluorescence, and ERG: electroretinography.

IS/OS: inner segment/outer segment layer, NA: not available.