Literature DB >> 25339260

Disease-specific growth charts for Korean infants with Prader-Willi syndrome.

Jieun Lee1, Tsuyoshi Isojima, Mi Sun Chang, Young Hee Kwun, Rimm Huh, Sung Yoon Cho, Young Bae Sohn, Dong-Kyu Jin.   

Abstract

Patients with Prader-Willi syndrome (PWS) present with short stature and obesity. The growth pattern of children with PWS is different from that of the healthy population. Therefore, it is not appropriate to use normal growth charts to evaluate the growth status of children with PWS. We aimed to develop disease-specific growth charts for height and weight for nongrowth hormone-treated Korean infants with PWS aged between 0 and 36 months and to use these growth charts for the evaluation and management of infants with PWS. We conducted a retrospective review of the medical records of 122 infants with genetically confirmed PWS. Data on the patients' height and weight measurements before they underwent growth hormone treatment were recorded. Disease-specific growth charts were generated and the 3rd, 10th, 25th, 50th, 75th, 90th, and 97th centiles were calculated using the LMS (refers to λ, μ, and σ, respectively) smoothing procedure for height and weight. The disease-specific growth charts for Korean infants with PWS can be used when examining infants with PWS and when evaluating their growth at later stages for comparison purposes. They are also useful for monitoring growth patterns, nutritional assessments, and recording responses to growth hormone treatment.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  Prader-Willi syndrome; body height; body weight; growth charts

Mesh:

Year:  2014        PMID: 25339260     DOI: 10.1002/ajmg.a.36816

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  2 in total

1.  Prader-Willi syndrome: an update on obesity and endocrine problems.

Authors:  Su Jin Kim; Sung Yoon Cho; Dong-Kyu Jin
Journal:  Ann Pediatr Endocrinol Metab       Date:  2021-12-31

2.  Growth charts for Thai children with Prader-Willi syndrome aged 0-18 years.

Authors:  Nantiya Mongkollarp; Thipwimol Tim-Aroon; Chusak Okascharoen; Khunton Wichajarn; Jeeraparn Phosuwattanakul; Nalinee Chongviriyaphan; Duangrurdee Wattanasirichaigoon
Journal:  Orphanet J Rare Dis       Date:  2020-05-06       Impact factor: 4.123

  2 in total

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