Weight for age charts for children with achondroplasia
β Scribed by J.E. Hoover-Fong; J. McGready; K.J. Schulze; H. Barnes; C.I. Scott
- Book ID
- 102701033
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 743 KB
- Volume
- 143A
- Category
- Article
- ISSN
- 1552-4825
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β¦ Synopsis
Abstract
To develop accurate weight for age charts for individuals with achondroplasia. These novel weight for age, genderβspecific growth curves for achondroplasia patients from birth through 16 years were constructed from a longitudinal, retrospective, single observer cohort study of 334 individuals with achondroplasia. Weight for age data from 301 subjects in this achondroplasia cohort, constituting 1,964 total weight measurements, are presented in these weight for age curves. Percentiles (5, 25, 50, 75, 95th) were estimated across the age continuum by gender, using a 1 month window (Β±0.5 months) around each time point of interest. Percentiles were smoothed using a quadratic, penalized smoother by a semiβparametric model approach. Raw weight data from the achondroplasia cohort are compared to that of average stature children presented in the current CDC growth curves, divided into 0β36 months and 2β16 years. There was overlap of birth weight between achondroplasia and average stature infants. This statistical modeling method can be applied to other anthropometric parameters collected from this achondroplasia cohort (e.g., length, BMI), other skeletal dysplasia diagnoses, and to syndromic, nonβskeletal dysplasia diagnoses which may benefit from standardization of weight for age. Β© 2007 WileyβLiss, Inc.
π SIMILAR VOLUMES
Standard curves developed for the general population cannot be used to assess the growth of an individual who has a condition that results in disproportionate short stature. For this reason, efforts have been made to develop growth curves specific for several of the chondrodysplasias. However, data
We previously reported on cognitive and respiratory factors in a series of infants with achondroplasia (ACH). We now present the results of neuropsychological evaluation and magnetic resonance imaging in 16 school-age children with ACH, 7 of whom had been included as infants in our previous report.
Because of gonadal mosaicism, the risk of recurrence of achondroplasia in the sibs of achondroplastic children with unaffected parents is presumably higher than twice the mutation rate, but it has not been measured.