Five cases with a cleft lip and/or palate and associated craniofacial bone anomalies were presented. In addition, the statistical frequency of the combination and the clinical management of such cases were discussed.
Case 1: A 7-y ear-old male had a unilateral cleft lip and a craniofacial cleft (Tessier type 10 cleft). Primary repair of the cleft lip was performed at the age of 3 months, and cranio-orbital (left) reconstruction was performed at the age of 30 months.
Case 2: A 6-year-old female had a uni l ateral cleft lip and palate and craniosynostosis (plagiocepha ly). Primary repair of the cleft lip and palate was performed at the age of 7 months and 23 months respectively, and cranio-supraorbital reconstruction was performed at the age of 42 months.
Case 3: A 4-year-old female had a median cleft lip and a craniofacial cleft (Tessier typ e 14 cleft). Anterior skull base reconstruction was performed at the age of 16 months, and primary repair of the median cleft lip was performed at the age of 40 months.
Case 4: A 3-year-old male had a median cleft lip and a craniosynostosis (trigonocephaly). Craniosupraorbital reconstruction was performed at the age of 17 months, and primary repair of the median cleft lip was performed at the age of 29 months.
Case 5: A 2-year-old female had an isolated cleft palate and craniosynostosis (trigonocephaly). Cranio-supraorbital reconstruction was performed at the age of 10 months, and primary repair of the cleft palate was performed at the age of 15 months.
Using Japanese statistical reports, craniofacial bon e anomalies were predicted to appear in 5% of all cleft lip and/or palate patients.
For the clinical management of these patients, considerations of appropriate diagnostic techniques, operative procedures for craniofacial surgery, and the timing for reconstruction of the anom alies must be made.
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