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. 2022 Nov 7;22:1142. doi: 10.1186/s12885-022-10235-w

Table 3.

Prevalence of KRAS, NRAS and BRAF mutations in North Africa

Country
Author [reference]
Gene frequency n/N (%) Exon frequency n/N (%)
KRAS NRAS BRAF KRAS Exon2 KRAS Exon3 KRAS Exon4 NRAS Exon2 NRAS Exon3 NRAS Exon4 BRAF Exon15
Morocco
 El Agy et al. [18] 77/210 (36.7%) 6/210 (2.9%) 0/210 (0%) 68 (83.3%) 1 (1.3%) 8 (10.4%) 2 (33.3%) 4 (66.7%) na na
 Houssaini et al. [19] 22/51 (43.1%) 1/51 (2%) 2/51 (3.9%) 26a (92.8%) na 2a (7.1%) na na na 2 (3.9%)
 Dehbi et al. [20] 49/114 (43%) 6/114 (5.3%) na 45 (91.8%) 3 (6.1%) 1 (2.04%) na 6 (5.3%) na na
 Jadda et al. [21] 24/47 (51%) na 0/47 (0%) 24 (51%) na na na na na 0 (0%)
 Marchoudi et al. [22] 22/92 (23.9%) na 5/92 (5.4%) 22/92 (23.9%) na na na na na 5 (5.4%)
 Bennani et al. [23] 18/62 (29%) na 1/62 (1.6%) 18 (38.7%) na na na na na 1 (1.6%)
Tunisia
 Ounissi et al. [24] 40/96 (41.7%) 7/96 (7.3%) na 47b (100%) na na 5c (62.5%) 3c (37.5%) 0c (0%) na
 Jouini et al. [25] 88/129 (68.2%) 9/129 (6.9%) na 84 (95.4%) 1 (1.1%) 3 (3.4%) 3 (33.3%) 4 (44.4%) 2 (22.2%) na
 Chaar et al. [26] 52/167 (31.1%) na na 52 (31.1%) na na na na na na
 Aissi et al. [27] 16/51 (31.5%) na na 16 (31.5%) na na na na na na
 Ouerhani et al. [28] 17/48 (35.41%) na na ni na na na na na na
 Sammoud et al. [29] 12/52 (23.1%) na na 12 (23.1%) na na na na na na
 Bougatef et al. [30] 22/48 (45.83%) na na 22 (45.83%) na na na na na na
 Bougatef et al. [31] na na 4/48 (8.3%) Na na na na na na 4 (8.3%)
Algeria
 Mazouzi et al. [32] 245/490 (50%) 6/490d (1.2%) na 237 (96.7%) 8 (3.3%) na na na na Na
 Boudida-Berkane K et al. [33] 32/102 (31.4%) na 5/102 (4.9%) 32 (31.4%) na na na na na 5 (4.9%)
Lybia
 Abudabous et al. [34] 13/34 (38.2%) na na 13 (38.2%) na na na na na na

na not available

aIn about 22 Patients with a KRAS mutations, 28 mutations were detected in exon 2 and exon 4 (Some patients have concomitant mutations)

bIn a total of 40 cases, we had 47 mutations in KRAS exon 2 (7/40 patients had 2 concomitant mutations in exon 2)

cOne of the 7 patients with NRAS mutation showed a double mutation in NRAS

dRare mutations in the NRAS gene