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. 2020 Jul 3;9(7):2097. doi: 10.3390/jcm9072097

Table 1.

Clinical characteristic of the 52 included patients.

Clinical Characteristics Study Population (n = 52)
Female, n (%) 29 (56%)
Ancestry, n (%)
  European 5 (9.6%)
  Sub-Saharan Africa/Caribbean 37 (71.15%)
  North African 9 (17.3%)
  India 1 (1.9%)
Age at diagnosis, in years, mean ± SD (rv) 12.03 ± 2.715 (5; 15)
Age at the last evaluation, in years, median (Q1–Q3) 23.6 (19.25–26.48)
Length of follow-up, in years, median (Q1–Q3) 11.48 (6.48;14.5)
Delayed diagnosed comorbidity, n (%)
  Crohn disease 2 (3.8%)
  Acquired hemophilia 1 (1.9%)
  Immune thrombocytopenia 1 (1.9%)
  Hemochromatosis 1 (1.9%)
  Idiopathic hemophagocytic lymphohistiocytosis 1 (1.9%)

SD: standard deviation, rv: range values, Q1: first quartile, Q3: third quartile.