Cornelia de Lange syndrome- Report of the Second Case from Ahvaz
Cornelia de Lange syndrome (CdLS) is a rare hereditary disease, characterized by severe growth retardation, microcephaly, and limb anomalies, distinctive dysmorphic features and mental retardation. The etiology is not still clear. However, it is caused by mutation of the nipped- B- like (NIPBL) gene...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | Persian |
| Published: |
Ahvaz Jundishapur University of Medical Sciences
2012-09-01
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| Series: | Majalah-i ̒ilmī pizishkī-i jundī/shapūr |
| Subjects: | |
| Online Access: | http://journals.ajums.ac.ir/components4.php?rQV===AfABDQ6QnchR3cfZGfABDNApDZJRnblJXYw9lZ8BkN3MDQ6QWStVGdp9lZ8BEOApDZJxWY0J3bQxWYuJXdvp2XmxHQyATNApDZJ52bpR3Yh9lZ |
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