A boy with growth and mental retardation, flat occiput, high and broad forehead, blepharoptosis, narrow palpebral fissures, low set, malformed ears, short neck, anal atresia, deep sacral dimple is reported. High-resolution banding analysis showed terminal deletion of the short arm of chromosome 3 (46,XY,del(3)(p25.3)). Deletions of the short arm of chromosome 3 are relatively rare. The clinical features of the patient are compared with those of 19 previously reported cases.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1007/BF01899740 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!