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J Postgrad Med ; 1994 Jan-Mar; 40(1): 40-1
Article in English | IMSEAR | ID: sea-115602

ABSTRACT

A 2 1/2 month old male child was admitted with loose motions and mild dehydration. He was full term normal delivery, born of a non-consanguinous marriage. On examination, he had trigonocephaly; anteverted nostrils, long philtrum and hypoplastic supraorbital ridges. X-ray showed sutural separation. Karyotyping confirmed deletion of short arm of chromosome 9 distal to band p22.


Subject(s)
Child, Preschool , Chromosome Deletion , Chromosomes, Human, Pair 9 , Craniofacial Dysostosis/etiology , Humans , Male , Skull/abnormalities , Syndrome
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