Cleft Lip and Palate
Cleft Lip and Palate
Cleft Lip and Palate
Introduction
lefts involving the lip and/or palate (CLP) or isolated clefts of the palate (CP) are
the most common congenital anomaly to affect the craniofacial region in man,
comprising about 65% of all anomalies affecting the head and neck.
2_A family history can be found in around 40% of cases of cleft lip with or without
cleft palate,
3_the risk of unaffected parents having another child with this anomaly is 1 in 25
4_Males are affected more frequently than females, and the left side is involved
more commonly than the right.
Aetiology األسباب
1_In normal development, fusion of the embryological processes that comprise
the upper lip occurs around the sixth week of intrauterine life
4_both genetic and environmental factors play a part in the aetiology of clefts.
5_Specific gene mutations have been shown to be linked to cleft lip and/or cleft
palate
7_t is postulated that isolated cleft palate is more common in females than
males because transposition of the palatal shelves occurs later in the
female fetus.
9_A number of possible causes of cleft lip and palate have been identified,
including exposure to some teratogens.
10 addition to “typical” cleft lip and cleft palate, unusual facial clefts occur that
also result from the failure of facial prominences to properly form or
unite.Examples include macrostomia,
11_a defect at the junction of the maxillary and mandibular prominences that
may result from a growth deficiency in either or both of these growth centers, and
oblique facial clefts that occur at the junction of the maxillary growth center with
either the lateral nasal or maxillary growth center.
Classification
1_CP can range from a simple submucous cleft (a lack of continuity of the
muscles across the palate) or bifid uvula to a complete cleft involving the primary
and secondary palate
2_CLP can range from simple notching or isolated clefting of the upper lip with or
without involvement of the alveolus, to complete unilateral or bilateral clefts of the
lip, alveolus and hard/soft palate.
Treatment
1_A child born with orofacial clefting will require complex long-term treatment,
depending upon the severity of the cleft
4_Good hearing.
Problems In Management
1_Congenital Anomalies
The disturbances in dental and skeletal development caused by the clefting
process itself depend upon the site and severity of the cleft
2_Lip Only
There is little effect in this type, although notching of the alveolus adjacent to the
cleft lip may sometimes be seen
1 Congenital absence .
2_ilateral clefts, both lateral segments are often collapsed behind a prominent
premaxilla
5_Palate Only
1 A widening of the arch posteriorly is usually seen. It has been shown that
individuals with a cleft have a more concave profile,
3 more retrognathic maxilla and mandible and also a reduced upper face height