3p Deletion Syndrome.
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Date
2013-08
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Abstract
3p deletion is a rare cytogenetic finding. Here we describe a 3 months old male with
congenital malformations. His karyotype revealed 3p deletion 46,XY,del(3)(p25-pter). The
child had flexion deformity of wrist and elbow which has never been reported before.
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Keywords
3p deletion, trignocephaly, micrognathia
Citation
Kaur Anupam, Khetarpal S. 3p Deletion Syndrome. Indian Pediatrics. 2013 August; 50(8): 795.