| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4142178 | Anales de Pediatría | 2011 | 4 Pages |
Abstract
Knowledge of this condition has therapeutic implications, given the favourable progress with growth hormone treatment, as well as possible surgical procedures and genetic counselling, due to its autosomal dominant hereditary character.
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Authors
I. Llano-Rivas, J. Fernández-Toral, I. Navarro-Vera,