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Journal Français d'Ophtalmologie
Vol 26, N° 7  - septembre 2003
pp. 738-742
Doi : JFO-09-2003-26-7-0181-5512-101019-ART13
Le syndrome d'Apert : à propos d'une observation
Figure 1

Figure 1. Exophtalmie bilatérale avec ectropion supérieur et inférieur gauche.
Figure 2

Figure 2. Hypoplasie maxillaire et prognathisme mandibulaire.
Figure 3

Figure 3A

Figure 3B

Figure 3. Syndactylie des 2 e , 3 e et 4 e doigts.
Figure 4

Figure 4A

Figure 4B

Figure 4. Syndactylie des 3 e , 4 e et 5 e orteils.
Figure 5

Figure 5. Impressions digitiformes frontales.
Figure 6

Figure 6. Hypoplasie maxillaire et prognathisme mandibulaire.
Figure 7

Figure 7. Cardiomégalie et horizontalité costale.
Figure 8

Figure 8. Profil électrophorétique de la mutation du gène FGFR2 chez la patiente 3.

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