Literature DB >> 15688383

Scoliosis in CHARGE: a prospective survey and two case reports.

Crystal Doyle1, Kim Blake.   

Abstract

CHARGE syndrome was first identified as a cluster of congenital anomalies in 1979 and has since undergone diagnostic criteria modifications to include the major and minor characteristics that occur during infancy and childhood. As the individuals with CHARGE syndrome have aged into their adolescents and adulthood, it has become increasingly common for them to develop scoliosis. This article presents an older population of individuals with CHARGE syndrome and describes the prevalence of scoliosis, and identifiable risk factors for scoliosis. Two case reports demonstrate the variability of scoliosis in CHARGE syndrome. A survey of adults and adolescents with CHARGE syndrome was completed to collect information about late onset medical issues, and those identifying scoliosis as an issue, were further followed for more information. The total population (n=31) and then the subgroup of individuals with scoliosis (n=19) were analyzed. Sixty one percent (19 of 31) of this population was diagnosed with scoliosis. The age of CHARGE syndrome diagnosis was later in the scoliosis population (6.3 years compared to 3.7 years in the no scoliosis population). Growth hormone use was reported in 7 of 31 of the individuals; 6 of these subsequently were diagnosed with scoliosis (32% of the scoliosis group). Of the scoliosis subgroup, most were mild scoliosis but eight were diagnosed with moderate to severe scoliosis, and all of these were treated with either a brace (n=5) or with surgical fusion (n=2) and one individual had both. Scoliosis in CHARGE syndrome individuals is more common than previously reported, and the age of onset is earlier than when routine monitoring for scoliosis is recommended. The prevalence of scoliosis in the CHARGE syndrome population is higher than in the general population therefore, it is very important for physicians to carefully monitor the spine for the development of scoliosis in children with CHARGE syndrome, especially if they are being treated with growth hormone. Copyright (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15688383     DOI: 10.1002/ajmg.a.30564

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


  9 in total

1.  Atypical phenotypes associated with pathogenic CHD7 variants and a proposal for broadening CHARGE syndrome clinical diagnostic criteria.

Authors:  Caitlin L Hale; Adrienne N Niederriter; Glenn E Green; Donna M Martin
Journal:  Am J Med Genet A       Date:  2015-11-21       Impact factor: 2.802

2.  Juvenile Muscular Atrophy of a Unilateral Upper Extremity (Hirayama Disease) in a Patient with CHARGE Syndrome.

Authors:  T Yagihashi; K Hatori; K Ishii; C Torii; S Momoshima; T Takahashi; K Kosaki
Journal:  Mol Syndromol       Date:  2010-06-30

Review 3.  CHARGE syndrome.

Authors:  Kim D Blake; Chitra Prasad
Journal:  Orphanet J Rare Dis       Date:  2006-09-07       Impact factor: 4.123

4.  CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis.

Authors:  Xiaochong Gao; Derek Gordon; Dongping Zhang; Richard Browne; Cynthia Helms; Joseph Gillum; Samuel Weber; Shonn Devroy; Saralove Swaney; Matthew Dobbs; Jose Morcuende; Val Sheffield; Michael Lovett; Anne Bowcock; John Herring; Carol Wise
Journal:  Am J Hum Genet       Date:  2007-03-12       Impact factor: 11.025

5.  Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.

Authors:  Swarkar Sharma; Xiaochong Gao; Douglas Londono; Shonn E Devroy; Kristen N Mauldin; Jessica T Frankel; January M Brandon; Dongping Zhang; Quan-Zhen Li; Matthew B Dobbs; Christina A Gurnett; Struan F A Grant; Hakon Hakonarson; John P Dormans; John A Herring; Derek Gordon; Carol A Wise
Journal:  Hum Mol Genet       Date:  2011-01-07       Impact factor: 6.150

6.  Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis.

Authors:  Shashikant Kulkarni; Prabakaran Nagarajan; Jonathan Wall; Diana J Donovan; Robert L Donell; Azra H Ligon; Sundaresan Venkatachalam; Bradley J Quade
Journal:  Am J Med Genet A       Date:  2008-05-01       Impact factor: 2.802

Review 7.  Guidelines in CHARGE syndrome and the missing link: Cranial imaging.

Authors:  Christa M de Geus; Rolien H Free; Berit M Verbist; Deborah A Sival; Kim D Blake; Linda C Meiners; Conny M A van Ravenswaaij-Arts
Journal:  Am J Med Genet C Semin Med Genet       Date:  2017-11-23       Impact factor: 3.908

8.  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

9.  An N-Ethyl-N-Nitrosourea (ENU) Mutagenized Mouse Model for Autosomal Dominant Nonsyndromic Kyphoscoliosis Due to Vertebral Fusion.

Authors:  Christopher T Esapa; Sian E Piret; M Andrew Nesbit; Gethin P Thomas; Leslie A Coulton; Orla M Gallagher; Michelle M Simon; Saumya Kumar; Ann-Marie Mallon; Ilaria Bellantuono; Matthew A Brown; Peter I Croucher; Paul K Potter; Steve Dm Brown; Roger D Cox; Rajesh V Thakker
Journal:  JBMR Plus       Date:  2018-03-08
  9 in total

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