RT Journal Article SR Electronic T1 Deletion of the short arm of chromosome No. 10. JF Journal of Medical Genetics JO J Med Genet FD BMJ Publishing Group Ltd SP 99 OP 103 DO 10.1136/jmg.12.1.99 VO 12 IS 1 A1 M H Shokeir A1 M Ray A1 J L Hamerton A1 F Bauder A1 H O'Brien YR 1975 UL http://jmg.bmj.com/content/12/1/99.abstract AB A newborn male infant, whose karyotype was 46,XY,del(10)(p13) is presented. The clinical features included cleft lip and palate, preauricular pits, low set malpositioned auricles, antimongoloid slant of the eyes, microcephaly, micrognathia, congenital heart disease, hypertrophic pyloric stenosis, cryptorchidism, and abnormal dermatoglyphics. The child died at the age of 3 months in overwhelming urinary infection with septicemic complications. It is suggested that the features described here may represent a new, clinically recognizable chromosomal syndrome.