1.
Indian Pediatr
;
2013 August; 50(8): 795
Article
in English
| IMSEAR
| ID: sea-169939
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.