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CLEFT LIP AND
CLEFT PALATE
BY: JAYA SHARMA FATIMA COLLEGE OF NURSING
INTRODUCTION
 Cleft lip and cleft palate are congenital
malformations of face resulting from the failure
of fusion of first branchial arch during
intrauterine development .
 The complete formation of lip often occurs by
5 to 12 weeks ,whereas the formation of palate
may occur only by 12 to 14 weeks of
gestational age.
 These conditions are usually detected at birth
and may be associated with other congenital
anomalies in about 20% of cases .
 Cleft lip and cleft palate may occur as single or
in combination .it may be unilateral or bilateral.
CLEFT LIP
 It results from failure of the maxillary process
to fuse with nasal elevations on frontal
prominence .
 The extent of cleft lip is varying from a notch
in the vermilion border to a large cleft reaching
the floor of the nose .
 It is apparent at birth as incomplete formation
of lips.
 It may be associated with cleft palate and
supernumerary, deformed or absent teeth .
CLEFT PALATE
 It results from failure of masses of lateral
palatine processes to meet and fuse together .
 It is unilateral or bilateral and in isolation and
found in the midline involving only uvula or
reaches the incisive foramen through soft
palate .
 CP is found as an opening or elongated
opening or fissure in the roof of the mouth .
CAUSES
GENETICS
MATERNAL
FACTOR
INFECTION
ANEMIA
HYPOPROTEINEMIA
TYPES OF CLEFT LIP AND
PALATE
COMPLICATION
 IMMIDIATE PROBLEM :-
1. Feeding problem
2. Aspiration
3. Parental anxiety
 LONG TERM PROBLEM
 Recurrent infection
 Disturbed parent child relationship
 Impairment of speech
 Hearing problem
 Impaired body image
SURGICAL MANGEMENT
 Cheiloplasty
 Palatoplasty

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cleft lip and cleft palate.pptx

  • 1. CLEFT LIP AND CLEFT PALATE BY: JAYA SHARMA FATIMA COLLEGE OF NURSING
  • 2. INTRODUCTION  Cleft lip and cleft palate are congenital malformations of face resulting from the failure of fusion of first branchial arch during intrauterine development .  The complete formation of lip often occurs by 5 to 12 weeks ,whereas the formation of palate may occur only by 12 to 14 weeks of gestational age.  These conditions are usually detected at birth and may be associated with other congenital anomalies in about 20% of cases .
  • 3.  Cleft lip and cleft palate may occur as single or in combination .it may be unilateral or bilateral.
  • 4. CLEFT LIP  It results from failure of the maxillary process to fuse with nasal elevations on frontal prominence .
  • 5.  The extent of cleft lip is varying from a notch in the vermilion border to a large cleft reaching the floor of the nose .  It is apparent at birth as incomplete formation of lips.  It may be associated with cleft palate and supernumerary, deformed or absent teeth .
  • 6.
  • 7. CLEFT PALATE  It results from failure of masses of lateral palatine processes to meet and fuse together .  It is unilateral or bilateral and in isolation and found in the midline involving only uvula or reaches the incisive foramen through soft palate .  CP is found as an opening or elongated opening or fissure in the roof of the mouth .
  • 8.
  • 10. TYPES OF CLEFT LIP AND PALATE
  • 11. COMPLICATION  IMMIDIATE PROBLEM :- 1. Feeding problem 2. Aspiration 3. Parental anxiety
  • 12.  LONG TERM PROBLEM  Recurrent infection  Disturbed parent child relationship  Impairment of speech  Hearing problem  Impaired body image