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. 2020 Jan 30;98(5):464–471. doi: 10.1111/aos.14360

Table 2.

Demographics and ocular status of patients with ocular von Hippel–Lindau disease.

    Missense mutation carriers (n = 6) Truncating mutation carriers (n = 15) p
Sex Male/female 3/3 6/9  
Age at baseline visit (years), mean ± SD   22.4 ± 10.3 26.7 ± 16.4 0.570
Age of diagnosis RHs (years), mean ± SD   26.1 ± 8.1 25.5 ± 15.5 0.931
Follow‐up duration (years), mean ± SD   19.4 ± 7.4 15.1 ± 10.6 0.383
Ocular status, n Unilateral involvement 2 5  
  Bilateral involvement 4 10  
  Severe involvement 2 1