Abstract
The first textbook of Pediatric Endocrinology in the early 1950s reported an association of neurofibromatosis type 1 (NF1) and precocious puberty (PP) and/or short stature. Recent studies have indicated that children with NF1 grow normally until puberty; thereafter height velocity and relative height (SDS or percentiles) decreases with respect to healthy peers, reaching a mean adult height close to the 25th percentile for the general population. Moreover, the percentage of patients with true short stature (2 SD): 16% vs 6.8% (mothers) vs 3.4% (controls) (p
Original language | English |
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Pages (from-to) | 289-292 |
Number of pages | 4 |
Journal | Journal of Pediatric Endocrinology and Metabolism |
Volume | 16 |
Issue number | SUPPL. 2 |
Publication status | Published - 2003 |
Keywords
- Delayed puberty
- GnRH agonist therapy
- Growth
- Neurofibromatosis type 1
- Optic gliomas
- Optic pathway tumors
- Precocious puberty
ASJC Scopus subject areas
- Endocrinology
- Pediatrics, Perinatology, and Child Health