Abstract
A male premature infant presented with slow development and congenital camptodactyly of both hands. Chromosome analysis showed a 48,XXYY karyotype. As far as we know, this is the first report describing congenital camptodactyly associated with the 48,XXYY syndrome
| Original language | English |
|---|---|
| Pages (from-to) | 19-21 |
| Journal | Genetic counseling (Geneva, Switzerland) |
| Volume | 9 |
| Issue number | 1 |
| Publication status | Published - 1998 |