Literature DB >> 23165933

Functional independence of Taiwanese children with VACTERL association.

Hsin-Yi Lin1, Shuan-Pei Lin, Hsiang-Yu Lin, Chyong-Hsin Hsu, Jui-Hsing Chang, Hsin-An Kao, Han-Yang Hung, Chun-Chih Peng, Hung-Chang Lee, Ming-Ren Chen, Jeng-Daw Tsai.   

Abstract

VACTERL association is a non-random association of birth defects, which may include anomalies of the vertebral column, limbs, kidneys, and heart; anal atresia; tracheoesophageal fistula; and esophageal atresia. The presence of two or more of the defects establishes the diagnosis. The aim of our study is to describe the functional independence of children with VACTERL association and compare the results to unaffected children. These results will enable clinicians to provide more realistic prognostic information to parents and families. We used the WeeFIM questionnaire to assess the functional skills of 23 patients who had been diagnosed with VACTERL association at Mackay Memorial Hospital, Taipei, Taiwan, from June 1994 to June 2009. The total WeeFIM scores and sub-scores for three domains (self-care, mobility, and cognition) correlated significantly with age (P < 0.01). The scores were generally within the same range as those of unaffected Chinese children, although our subjects had slightly inferior scores on six items, including bowel, chair transfer, stairs, expression, social interaction, and problem solving. In conclusion, the daily functional skills of Taiwanese children with VACTERL association were similar to those of unaffected children.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 23165933     DOI: 10.1002/ajmg.a.33643

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


  4 in total

1.  Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genes.

Authors:  Caroline M Kolvenbach; Amelie T van der Ven; Franziska Kause; Shirlee Shril; Marcello Scala; Dervla M Connaughton; Nina Mann; Makiko Nakayama; Rufeng Dai; Thomas M Kitzler; Ronen Schneider; Luca Schierbaum; Sophia Schneider; Andrea Accogli; Annalaura Torella; Gianluca Piatelli; Vincenzo Nigro; Valeria Capra; Bernd Hoppe; Stefanie Märzheuser; Eberhard Schmiedeke; Heidi L Rehm; Shrikant Mane; Richard P Lifton; Gabriel C Dworschak; Alina C Hilger; Heiko Reutter; Friedhelm Hildebrandt
Journal:  Am J Med Genet A       Date:  2021-08-02       Impact factor: 2.578

2.  Functional independence of Taiwanese patients with mucopolysaccharidoses.

Authors:  Chung-Lin Lee; Hsiang-Yu Lin; Chih-Kuang Chuang; Huei-Ching Chiu; Ru-Yi Tu; You-Hsin Huang; Wuh-Liang Hwu; Fuu-Jen Tsai; Pao-Chin Chiu; Dau-Ming Niu; Yann-Jang Chen; Mei-Chyn Chao; Tung-Ming Chang; Ju-Li Lin; Chia-Ying Chang; Yu-Chia Kao; Shuan-Pei Lin
Journal:  Mol Genet Genomic Med       Date:  2019-06-18       Impact factor: 2.183

3.  Study of Nursing Models by Machine Learning in Children with Congenital Esophageal Atresia.

Authors:  Yu Zhang; Xueqiang Sun; Jingyun Shi; Zhenjuan Xiao
Journal:  Comput Intell Neurosci       Date:  2022-04-10

4.  Functional Independence of Taiwanese Children with Osteogenesis Imperfecta.

Authors:  Yu-Min Syu; Chung-Lin Lee; Chih-Kuang Chuang; Huei-Ching Chiu; Ya-Hui Chang; Hsiang-Yu Lin; Shuan-Pei Lin
Journal:  J Pers Med       Date:  2022-07-24
  4 in total

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