Literature DB >> 18059083

Early diagnosis and multidisciplinary care reduce the hospitalization time and duration of tube feeding and prevent early obesity in PWS infants.

N Bacheré1, G Diene, V Delagnes, C Molinas, P Moulin, M Tauber.   

Abstract

BACKGROUND/AIMS: To describe and evaluate the impact of very early diagnosis and multidisciplinary care on the evolution and care of infants presenting with Prader-Willi syndrome (PWS).
METHODS: 19 infants diagnosed with PWS before the second month of life were followed by a multidisciplinary team. Median age at the time of analysis was 3.1 years [range 0.4-6.5]. The data were compared with data collected in 1997 from 113 questionnaires filled out by members of the French PWS Association. The patients from this latter data set were 12.0 years [range 4 months to 41 years] at the time of analysis, with a median age of 36 months at diagnosis.
RESULTS: The duration of their hospitalization time was significantly reduced from 30.0 [range 0-670] to 21 [range 0-90] days (p = 0.043). The duration of gastric tube feeding was significantly reduced from 30.5 [range 0-427] to 15 [range 0-60] days (p = 0.017). Growth hormone treatment was started at a mean age of 1.9 +/- 0.5 years in 10 infants and L-thyroxine in 6 infants. Only 1 infant became obese at 2.5 years.
CONCLUSION: Early diagnosis combined with multidisciplinary care decreases the hospitalization time, duration of gastric tube feeding and prevents early obesity in PWS infants. (c) 2007 S. Karger AG, Basel.

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Year:  2007        PMID: 18059083     DOI: 10.1159/000111795

Source DB:  PubMed          Journal:  Horm Res        ISSN: 0301-0163


  20 in total

1.  PET scan perfusion imaging in the Prader-Willi syndrome: new insights into the psychiatric and social disturbances.

Authors:  Carine Mantoulan; Pierre Payoux; Gwenaëlle Diene; Mélanie Glattard; Bernadette Rogé; Catherine Molinas; Annick Sevely; Monica Zilbovicius; Pierre Celsis; Maïthé Tauber
Journal:  J Cereb Blood Flow Metab       Date:  2010-06-30       Impact factor: 6.200

2.  Early Detection and Management of Prader-Willi Syndrome in Egyptian Patients.

Authors:  Hala T El-Bassyouni; Nagwa Hassan; Inas Mahfouz; Azza E Abd-Elnaby; Mostafa I Mostafa; Angie M S Tosson
Journal:  J Pediatr Genet       Date:  2019-08-04

3.  Systematic review of the clinical and genetic aspects of Prader-Willi syndrome.

Authors:  Dong Kyu Jin
Journal:  Korean J Pediatr       Date:  2011-02-28

Review 4.  Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China.

Authors:  Dai Yang-Li; Luo Fei-Hong; Zhang Hui-Wen; Ma Ming-Sheng; Luo Xiao-Ping; Liu Li; Wang Yi; Zhou Qing; Jiang Yong-Hui; Zou Chao-Chun
Journal:  Orphanet J Rare Dis       Date:  2022-06-13       Impact factor: 4.303

5.  [Clinical screening and genetic diagnosis for Prader-Willi syndrome].

Authors:  Guo-Qing Dong; Yue-Yue Su; Xiao-Ying Qiu; Xi-Yan Lu; Jian-Xu Li; Miao Huang; Xiao-Ping Luo
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2020-09

6.  Scoliosis in patients with Prader Willi Syndrome - comparisons of conservative and surgical treatment.

Authors:  Hans-Rudolf Weiss; Deborah Goodall
Journal:  Scoliosis       Date:  2009-05-06

7.  Clinical and genetic analysis for four Chinese families with Prader-Willi syndrome.

Authors:  Yu-wen Zhang; Hui-ying Jia; Jie Hong; Yan Ge; Hui-jie Zhang; Chun-fang Shen; Lei Ye; Bin Cui; Xiao-ying Li; Wei-qiong Gu; Yi-fei Zhang; Wei-qing Wang; Guang Ning
Journal:  Endocrine       Date:  2009-05-07       Impact factor: 3.633

8.  Highly restricted deletion of the SNORD116 region is implicated in Prader-Willi Syndrome.

Authors:  Eric Bieth; Sanaa Eddiry; Véronique Gaston; Françoise Lorenzini; Alexandre Buffet; Françoise Conte Auriol; Catherine Molinas; Dorothée Cailley; Caroline Rooryck; Benoit Arveiler; Jérome Cavaillé; Jean Pierre Salles; Maïthé Tauber
Journal:  Eur J Hum Genet       Date:  2014-06-11       Impact factor: 4.246

9.  Correlation of Genotype and Perinatal Period, Time of Diagnosis and Anthropometric Data before Commencement of Recombinant Human Growth Hormone Treatment in Polish Patients with Prader-Willi Syndrome.

Authors:  Agnieszka Lecka-Ambroziak; Marta Wysocka-Mincewicz; Katarzyna Doleżal-Ołtarzewska; Agata Zygmunt-Górska; Teresa Żak; Anna Noczyńska; Dorota Birkholz-Walerzak; Renata Stawerska; Maciej Hilczer; Monika Obara-Moszyńska; Barbara Rabska-Pietrzak; Elżbieta Gołębiowska; Adam Dudek; Elżbieta Petriczko; Mieczysław Szalecki
Journal:  Diagnostics (Basel)       Date:  2021-04-28

10.  French database of children and adolescents with Prader-Willi syndrome.

Authors:  Catherine Molinas; Laurent Cazals; Gwenaelle Diene; Melanie Glattard; Catherine Arnaud; Maithe Tauber
Journal:  BMC Med Genet       Date:  2008-10-02       Impact factor: 2.103

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