Lecture Craniofacial Limoudei Hemsech

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18 Apert cont • Mild telorbitism, midfacial retrusion, deficient maxilla, abnormal dentition, Cleft palate 11-30%, low hair line, hypertrichosis of the eye brows, ptosis (mainly lateral), well developed protruding tongue. • Mental reardation seen in most.
19 Pfeiffer (Acrocephalosyndactyly, type V) • Autosomal dominant (Most cases sporadic) Chromosome 8 • Brachy-turricephalic, broad thumbs and great toes, occasional minor syndactyly,maxillary retrusion, possible high arched palate and submucous cleft. • Intelligence normal to mild mental retardation.
Page 1 and 2: 1 Lecture Congenital Craniofacial P
Page 3 and 4: 3 Simple: involves the cranial sutu
Page 6 and 7: 6 ICP • Increased ICP is seen in
Page 8 and 9: 8 Visual abnormalities • Optic at
Page 10 and 11: 10 Brachycephaly AP shortening, for
Page 12 and 13: 12 Trigonocephaly Narrow and sharp
Page 14 and 15: 14 Plagiocephaly •Positional caus
Page 16 and 17: 16 Crouzon (Craniofacial dysostosis
Page 20 and 21: 20 Sathre-Chotzen (Acrocephalosynda
Page 22 and 23: 22 Classification of Tessier • Th
Page 24 and 25: 24 Clasification of Van der Mulen
Page 26 and 27: 26 Frontoethmoidal Encephalomeningo
Page 28 and 29: 28 Treacher Collins • Bilateral a
Page 30 and 31: 30 Nager syndrome (Acrofacial Dysos
Page 33 and 34: 33 Hemifacial microsomia • No gen
Page 35 and 36: 35 Romberg’s disease (Progresive
Page 37 and 38: 37 Pre operative evaluation • His
Page 39 and 40: 39 • Extensive use of bone grafts
Page 43 and 44: 43 Correction of syndromatic sutura
Page 45 and 46: 45 Forehead Advancement Forehead Ad
Page 47 and 48: 47 Forehead Advancement for Trigono
Page 49: 49 Complications • Infection of s

Lecture Craniofacial Limoudei Hemsech

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