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Table 1 General characteristics of the 357 children with neurofibromatosis-1 included in the study

From: Clinical characteristics predicting internal neurofibromas in 357 children with neurofibromatosis-1: results from a cross-selectional study

Clinical characteristics (n = missing data)

n (%)

Male gender

192 (53.8)

Age at the first visit in years, mean ± SD (range)

7.7 ± 5.0 (0.01-16.9)

Familial case

183 (51.3)

Internal neurofibromas

35 (9.8)

Subcutaneous neurofibromas (n = 17)

72 (20.2)

Cutaneous neurofibromas

153 (42.9)

Plexiform neurofibromas (n = 184)

83 (23.3)

Café-au-lait spots

354 (99.2)

Freckles (n = 11)

219 (61.3)

Lisch nodules (n = 84)

160 (44.8)

Xanthogranulomas (n = 68)

14 (3.9)

Short stature (n = 32)

36 (10.1)

Macrocephaly (n = 21)

85 (23.8)

Nonunion

13 (3.6)

Dysplasia (n = 8)

31 (8.7)

Facial asymmetry (n = 72)

23 (6.4)

Hypertension (n = 28)

3 (0.8)

  1. The data are number (%) unless otherwise specified.