CP

1.*******Write an essay on Craniofacial DO.**DO for facial deformi8es.

2.* Give a detailed account of ver8cal maxillary excess.
3.Discuss the management of bimaxillary prognathism with apertognathia.
4. **Discuss the comprehensive and current concepts of cleE lip and palate deformi8es.
5.*Discuss in detail complica8ons of orthognathic surgeries.
6.Discuss the diagnosis and management ow will you assess such a pa8ent? Discuss your
surgical management.
92. Enumerate the common craniofacial syndromes affec8ng the head and neck. Discuss the
management of a pa8ent with Crouzon syndrome from birth.
93.A pa8ent reports to the hospital with a history of deformity on one side of the face.What
is your diagnosis? Discuss the management of the pa8ent.
94. A pa8ent reports with anterior dental proclina8on. How would you treat the pa8ent
surgically if the mesial show was more than 5mm and less than 5mm? Discuss the full work
up and surgical op8ons for the pa8ent?
95.What is DO? Discuss in detail the treatment for a 10 year old boy with severe mandibular
hypoplasia using distrac8on. Add a note comparing DO to conven8onal OGS.
96. (SN)
a) Ant max. osteotomies types
b)Ant. Segmental osteotomy of the mandible
c)Presurgical Orthodon8cs- Treatment,aims,dura8on
d)3 D Virtual reconstruc8on with regards to OGS
e) Hemifacial microsomia
f) Aperts syndrome
g)Complica8ons following OGS
h)Psychological assessment of pa8ents undergoing OGS
i)Burstone Analysis/COGS
j)Alar cinching
k)The cleE palate pa8ent- surgical considera8on
l) SoE 8ssue changes following OGS
m)Func8onal indica8ons for OGS: including access osteotomies
n)CPAP versus maxillo mandibular advancement for OSA.
o)CleE lip and palate treatment protocol
P) Secondary cleE surgery
q)Naso alveolar moulding
r)Embryogenesis,e8ology and theories of CL & CP
s)Surgical treatment of cleE lip
t)Surgical treatment of cleE palate.