Embryo S2 ( week 1-6 )

bon courage mv

Pharyngeal Arches are
separated
one from the other
by the Pharyngeal Folds and
Pharyngeal Pouches on the
inside ( third week )

BIRTH DEFECTS-PERSISTENT BUCCOPHARYNGEAL MEMBRANE

PERSISTENT BUCCOPHARYNGEAL MEMBRANE

PERSISTENT BUCCOPHARYNGEAL MEMBRANE
WITH CLEFT PALATE

PERSISTENT BUCCOPHARYNGEAL MEMBRANES

PHARYNGEAL ARCH DEVELOPMENT ( the
frontonasal prominence and the paired
maxillary and mandibular prominences )

BILATERAL MACROSTOMIA

BILATERAL MACROSTOMIA WITH FACIAL TAGS

BILATERAL MACROSTOMIA and rigth BILATERAL MACROSTOMIA WITH FACIAL
TAGS

UNILATERAL MACROSTOMIA

SEVERE MICROSTOMIA

SEVERE MICROSTOMIA

FACIAL PRIMORDIA DEVELOPMENT

DEVELOPMENT OF THE FACE

CHIN DIMPLE-ARROWS

Large Pharyngeal/Branchial cyst-Arrow

PHARYNGEAL ARCH FISTULA

PHARYNGEAL ARCH FISTULA-ARROWS

PHARYNGEAL ARCH CYST-ARROWS

PHARYNGEAL ARCH CYST

PHARYNGEAL ARCH CYSTS-ARROWS

PIERRE ROBIN SEQUENCE/SYNDROME

PIERRE ROBIN SEQUENCE/SYNDROME

PIERRE ROBIN SEQUENCE/SYNDROME

PIERRE ROBIN SEQUENCE/SYNDROME

PIERRE ROBIN SEQUENCE/SYNDROME

PIERRE ROBIN SEQUENCE/SYNDROME

First arch syndrome ( PIERRE ROBIN SEQUENCE/SYNDROME )

Craniofacial Anomaly : Pierre Robin

PIERRE ROBIN SEQUENCE/SYNDROME

Treacher-Collins syndrome ( TCS )

Prenatal Diagnosis of Treacher-Collins syndrome ( TCS )

TREACHER COLLINS SYNDROME

TREACHER COLLINS SYNDROME-PRENATAL 3D DIAGNOSIS

TREACHER COLLINS SYNDROME

TREACHER COLLINS SYNDROME

TREACHER COLLINS SYNDROME

TREACHER COLLINS SYNDROME

Patients with TCS at different ages with visible variations in defect severity

GOLDENHAR SYNDROME

Micrognathia in an infant with Goldenhar's syndrome (hemifacial
microsomia)

GOLDENHAR SYNDROME WITH VISIBLE VARIATIONS IN DEFECT SEVERITY

GOLDENHAR SYNDROME or
OCULOAURICULOVERTEBRAL
DYSPLASIA and
HEMIFACIAL MICROSOMIA

GOLDENHAR SYNDROME WITH VISIBLE VARIATIONS IN DEFECT SEVERITY

ACROFACIAL DYSOSTOSIS SYNDROME

ACROFACIAL DYSOSTOSIS RODRIGUEZ TYPE
SYNDROME

Nager Acrofacial
Dysostosis is a
genetic disorder

ACROFACIAL DYSOSTOSIS NAGER TYPE SYNDROME

NAGER TYPE SYNDROME

ACROFACIAL DYSOSTOSIS NAGER TYPE SYNDROME

ACROFACIAL DYSOSTOSIS NAGER TYPE SYNDROME

MILLER SYNDROME

MILLER SYNDROME

MILLER SYNDROME

Miller Syndrome

MILLER SYNDROME

POSTAXIAL ACROFACIAL DYSOSTOSIS

CROUZON SYNDROME

CROUZON SYNDROME

CROUZON SYNDROME

CROUZON SYNDROME

CROUZON SYNDROME

TREACHER COLLINS SYNDROME

OROFACIAL CLEFTS

PALATAL DEVELOPMENT

NORMAL PALATAL DEVELOPMENT

NORMAL PALATAL DEVELOPMENT

CLEFT LIP-SURGICAL REPAIR OF THE LIP

A. and B. Unilateral-Left Cleft Lip and Cleft of the Primary and the
Secondary Palate

Unilateral-Left Cleft Lip and Cleft of the Primary Palate

Bilateral-Left Cleft Lip and Median Cleft Palate

Median cleft lip and median cleft palate

Bilateral-Left Cleft lip and Median Cleft Palate

Unilateral left cleft lip and cleft palate

Unilateral left cleft lip and cleft nasal cavity

Bifid/Cleft Uvula

cleft Uvula

Median Cleft Lip and Median Cleft Palate

Unilateral left cleft lip and cleft palate before and after surgical restoration

Unilateral-Right Cleft Lip and Cleft Palate

Unilateral-Left Cleft Lip and Cleft Palate-Before and after Surgical Restoration

Median Cleft Lip and Nasal Cavity Defect

Unilateral-Right Cleft Lip and Cleft
Palate

Unilateral-Left Cleft Lip and Cleft Palate-Before and after
Surgical Restoration

MEDIAN CLEFT PALATE

Stillborns with Median Cleft Lip and Median Cleft Palate

MEDIAN CLEFT LIP & CLEFT PALATE

BILATERAL CLEFT LIP

BIFID UVULA WITH INCOMPLETE MEDIAN
CLEFT PALATE

INCOMPLETE MEDIAN
CLEFT PALATE

left MEDIAN CLEFT LIP & CLEFT PALATE

middleUNILATERAL CLEFT LIP

right MEDIAN CLEFT LIP & CLEFT PALATE

OROFACIAL CLEFTS-TESSIER CLEFTS

HEMIFACIAL MICROSOMIA

HEMIFACIAL MICROSOMIA IN
GOLDENHAR’S SYNDROME

HEMIFACIAL MICROSOMIA IN
GOLDENHAR’S SYNDROME

Hemifacial microsomia

CASES OF MICROGNATHIA

MICROGNATHIA

MICROGNATHIA IN CROUZON SYNDROME

Crouzon syndrome