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Monosomy and trisomy of 15q24-qter with cleft lip and palate

Authors :
Mikio Shimizu
Atsushi Abe
N. Sugiyama
Y. Hatano
Kenichi Kurita
T. Yokoi
M. Nakano
Source :
International Journal of Oral and Maxillofacial Surgery. 37:487-490
Publication Year :
2008
Publisher :
Elsevier BV, 2008.

Abstract

Chromosome 15 aberrations clinically present as facial dysmorphisms such as a prominent nose, low-set ears, micrognathia and a short neck; a cleft lip and palate have not been reported. This is the first reported case of de-novo terminal deletion at 15q24 with a cleft lip and palate and low-set ears. The baby boy had a complete cleft lip and palate on the left side and incomplete cleft lip and palate on the right. A chromosomal study revealed partial monosomy and trisomy of the long arm of chromosome 15, with a karyotype of 46,XY,add(15)(24q) de novo. Surgery for lip plasty was performed at 6 months old and for palate plasty at 1 year and 9 months. Both operations were uneventful, although preoperative and postoperative examinations showed high creatinine phosphokinase values. At 3 years old, mild mental retardation was observed, but his physical development was normal.

Details

ISSN :
09015027
Volume :
37
Database :
OpenAIRE
Journal :
International Journal of Oral and Maxillofacial Surgery
Accession number :
edsair.doi.dedup.....3182cb80fc95a610f77a77e0a79404ed
Full Text :
https://doi.org/10.1016/j.ijom.2007.10.003