Craniofacial anomalies

Cleft lip and cleft lip and palate are common facial malformations that arise early in embryonic development. Their prevalence follows a north-south gradient worldwide. Cleft lip is more common than cleft palate. Known risk factors include maternal diabetes, gestational hyperthermia, as well as environmental and genetic factors. These malformations may occur in isolation or in association with other malformations as part of a genetic, chromosomal, or teratogenic syndrome.

Cleft Lip and Cleft Palate

A cleft lip is a failure of the embryonic facial tissue to fuse, resulting in a loss of tissue in the upper lip. A cleft palate is a lack of tissue in the roof of the mouth, resulting in a communication between the nose and the mouth. Most often, cleft lip is unilateral and occurs twice as often on the left side as on the right. The incidence of cleft lip and cleft palate appears to vary among populations. Cleft lip, with or without cleft maxillopalatine, is twice as common in boys as in girls.

Register

Period

Births

Live births

Stillbirths (excluding IMG)

IMG

Total

Total prevalence/10,000 (95% CI)

Antilles

2011–2015

47,493

15

2

5

22

4.6 (2.9–7.0)

Auvergne

2011–2015

66,381

56

1

12

69

10.4 (8.1–13.2)

Brittany

2011–2015

179 180

121

30

151

8.4 (7.1–9.9)

Paris

2011–2015

128,915

57

2

24

83

6.6 (5.3–8.2)

Reunion

2011–2015

71,756

56

1

14

71

9.9 (7.7–12.5)

Rhône-Alpes

2011–2015

292,693

218

4

58

280

9.6 (8.5–10.8)

Source: French Registries of Congenital Anomalies, INSEE for births in 2011–2015

Cleft palate

A cleft palate is a gap in the roof of the mouth resulting in a connection between the nose and the mouth. The cause of an isolated cleft palate differs from that of an isolated cleft lip. The incidence of cleft palates appears to vary by population. Unlike cleft lips and cleft lip and palate, this condition is twice as common in girls as in boys.

Register

Period

Births

Live births

Stillbirths (excluding IMG)

IMG

Total

Total prevalence/10,000 (95% CI)

Antilles

2011–2015

47,493

14

3

17

3.6 (2.1–5.7)

Auvergne

2011–2015

66,381

42

1

9

52

7.8 (5.9–10.3)

Brittany

2011–2015

179 180

103

3

38

144

8.0 (6.8–9.5)

Paris

2011–2015

128,915

55

18

73

5.7 (4.4–7.1)

Reunion

2011–2015

71,756

41

1

1

43

6.0 (4.3–8.1)

Rhône-Alpes

2011–2015

292,693

167

1

46

214

7.3 (6.4–8.4)

Source: French Registries of Congenital Anomalies, INSEE for births in 2011–2015