Literature DB >> 25703429

Spontaneous postnatal growth is reduced in children with CHARGE syndrome.

Helmuth G Dörr1, Julia Madeja1, Claudia Junghans2.   

Abstract

AIM: There is a scarcity of data on postnatal growth in children with CHARGE syndrome, a genetic disorder. This study analysed spontaneous growth and weight in German children with CHARGE from birth to the age of 6 years.
METHODS: This was a retrospective analysis of 19 children, nine females and 10 males, using data from child health records. Standard deviation scores (SDS) were calculated based on Swiss references.
RESULTS: The median birthweight was 2950 g (-0.78 SDS), and the birth length was 49 cm (-0.5 SDS). There was a significant loss of median body length, at around 4 weeks of age from -0.5 to -2.3 SDS (p < 0.05). At 1 year, the median length was -2.6 SDS and it remained low until 5 years of age when the lowest value was found to be -2.8 SDS. There was a significant increase in median body mass index (BMI) from -1.15 SDS at 1 year to -0.15 SDS at 5 years (p < 0.01).
CONCLUSION: Children with CHARGE syndrome displayed almost normal length and weight data at birth, with just one of the 19 infants having below average length for gestational age. However, postnatal growth was retarded during infancy and childhood, and the increase in BMI-SDS did not correlate with growth. ©2015 Foundation Acta Paediatrica. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Genetic disease; Growth hormone deficiency; Postnatal growth; Short stature; birth size

Mesh:

Year:  2015        PMID: 25703429     DOI: 10.1111/apa.12980

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  3 in total

1.  An analysis of body proportions in children with CHARGE syndrome using photogrammetric anthropometry.

Authors:  Bas Penders; Dieuwerke R Dijk; Gianni Bocca; Luc J I Zimmermann; Conny M A van Ravenswaaij-Arts; Willem-Jan M Gerver
Journal:  Am J Med Genet A       Date:  2019-05-27       Impact factor: 2.802

2.  Phenotypic spectrum of patients with mutations in CHD7: clinical implications of endocrinological findings.

Authors:  Ja Hye Kim; Yunha Choi; Soojin Hwang; Gu-Hwan Kim; Han-Wook Yoo; Jin-Ho Choi
Journal:  Endocr Connect       Date:  2022-02-11       Impact factor: 3.335

Review 3.  Eyes on CHARGE syndrome: Roles of CHD7 in ocular development.

Authors:  Laura A Krueger; Ann C Morris
Journal:  Front Cell Dev Biol       Date:  2022-09-08
  3 in total

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