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| CASE REPORTS |
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| Year : 1994 | Volume
: 40
| Issue : 1 | Page : 40-1 |
9p-Syndrome.
J Boby, SC Karande, KR Lahiri, MK Jain, S Kanade
Dept of Paediatrics, Seth GS Medical College, Parel, Bombay, Maharashtra.
Correspondence Address:
J Boby
Dept of Paediatrics, Seth GS Medical College, Parel, Bombay, Maharashtra.
 Source of Support: None, Conflict of Interest: None  | Check |
PMID: 0008568717 
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.
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