Table 1 Summary of clinical and genetic characteristics of the cohort.

From: Retrospective Analysis of Structural Disease Progression in Retinitis Pigmentosa Utilizing Multimodal Imaging

Inheritance

Subjects

Proportion

Genes Implicated (# of Patients)

ARRP

41

50.6%

USH2A (2), PDE6B (2), PDE6A (2), CNGB1 (2), MERTK (2), MAK1 (1), NPHP1 (1), EYS (1), CRB1 (1), RGR (1), Unknown (26)

ADRP

24

29.6%

RHO (4), PRPF31 (3), RP1 (3), Unknown (14)

Usher Syndrome

12

14.8%

USH2A (5), GPR98 (1), PCDH15 (1), Unknown (5)

XLRP

4

5%

RPGR (3), Unknown (1)

  1. ARRP autosomal recessive retinitis pigmentosa, ADRP autosomal dominant retinitis pigmentosa, XLRP X-linked retinitis pigmentosa.
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