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CLEFT LIP AND PALATE: THE JOS EXPERIENCE
Abstract
Objective: To determine the pattern of occurrence of cleft lip/palate and the factors
that may have influenced treatment outcome.
Design: Descriptive Study.
Setting: Jos University Teaching Hospital, Jos, Nigeria.
Subject: This study included 107 consecutive patients with cleft lip/palate managed
between January 1991 and June 1997.
Main outcome measures: The pattern of occurrence of cleft lip/palate, the peculiarities
of the malformation in this environment as well as factors that influenced treatment
outcome.
Results: The 107 patients were aged between one day and twenty-six years at
presentation. There were three adults aged between 18 and 26 years with a mean of
22.3 years and 104 children with a mean age of 9.5 months. The male/female ratio was
1. 1:1, the anomaly was 2.4 times commoner on the left and the cleft lip alone was
the most frequent mode of presentation (52%). The incidence was higher in the 3rd
and 4th siblings. In 13% of these patients, there were other associated congenital
anomalies such as Van der Woude’s Syndrome, Down’s Syndrome and congenital heart
disease. Complications were noted in 16(14.9%) patients and these included dehiscence
after repair in 8(7.5%) patients, oronasal fistulae in 2(1.9%), nasal speech in 4(3.7%)
and hypertrophic scar in 2(1.9%). Eighty nine percent of these repairs were satisfactory
to the parents of the affected children. All the adult patients were satisfied with their
repair.
Conclusion: The low incidence of this anomaly in our environment may be due to underreporting
in the rural areas. Public enlightenment programs should help improve early
presentation.
that may have influenced treatment outcome.
Design: Descriptive Study.
Setting: Jos University Teaching Hospital, Jos, Nigeria.
Subject: This study included 107 consecutive patients with cleft lip/palate managed
between January 1991 and June 1997.
Main outcome measures: The pattern of occurrence of cleft lip/palate, the peculiarities
of the malformation in this environment as well as factors that influenced treatment
outcome.
Results: The 107 patients were aged between one day and twenty-six years at
presentation. There were three adults aged between 18 and 26 years with a mean of
22.3 years and 104 children with a mean age of 9.5 months. The male/female ratio was
1. 1:1, the anomaly was 2.4 times commoner on the left and the cleft lip alone was
the most frequent mode of presentation (52%). The incidence was higher in the 3rd
and 4th siblings. In 13% of these patients, there were other associated congenital
anomalies such as Van der Woude’s Syndrome, Down’s Syndrome and congenital heart
disease. Complications were noted in 16(14.9%) patients and these included dehiscence
after repair in 8(7.5%) patients, oronasal fistulae in 2(1.9%), nasal speech in 4(3.7%)
and hypertrophic scar in 2(1.9%). Eighty nine percent of these repairs were satisfactory
to the parents of the affected children. All the adult patients were satisfied with their
repair.
Conclusion: The low incidence of this anomaly in our environment may be due to underreporting
in the rural areas. Public enlightenment programs should help improve early
presentation.
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