Literature DB >> 20447494

Nutrition for children with epidermolysis bullosa.

Lesley Haynes1.   

Abstract

Optimization of resistance to infection, growth, sexual maturation, wound healing, and provision of the best possible overall quality of life are important management goals in children with epidermolysis bullosa. However, all these goals rely on the maintenance of optimal nutritional status, and achieving this is extremely challenging in the severe types of the disease. Strategies to improve nutritional status have the best chance of success when the dietitian or nutritionist works as an integral member of the multidisciplinary team and is well informed of patients' situations, family dynamics, and prognoses. Even the best-coordinated dietetic interventions may exert only limited impact. Copyright 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20447494     DOI: 10.1016/j.det.2010.01.010

Source DB:  PubMed          Journal:  Dermatol Clin        ISSN: 0733-8635            Impact factor:   3.478


  8 in total

Review 1.  Dystrophic epidermolysis bullosa: a review.

Authors:  Satoru Shinkuma
Journal:  Clin Cosmet Investig Dermatol       Date:  2015-05-26

2.  Nutritional outcomes in children with epidermolysis bullosa: the experiences of two centers in Korea.

Authors:  Kyu-Yeun Kim; Ran Namgung; Soon Min Lee; Soo Chan Kim; Ho Sun Eun; Min Soo Park; Kook In Park; Chul Lee
Journal:  Yonsei Med J       Date:  2014-01       Impact factor: 2.759

Review 3.  Nutritional aspects of children and adolescents with epidermolysis bullosa: literature review.

Authors:  Ana Paula Caio Zidorio; Eliane Said Dutra; Dryelle Oliveira Dias Leão; Izelda Maria Carvalho Costa
Journal:  An Bras Dermatol       Date:  2015 Mar-Apr       Impact factor: 1.896

Review 4.  Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases.

Authors:  Jemima E Mellerio; Maya El Hachem; Nathalia Bellon; Giovanna Zambruno; Hana Buckova; Rudolf Autrata; Carmen Salavastru; Tamara Caldaro; Celine Greco; Cristina Has; Christine Bodemer
Journal:  Orphanet J Rare Dis       Date:  2020-06-06       Impact factor: 4.123

Review 5.  Occupational therapy for epidermolysis bullosa: clinical practice guidelines.

Authors:  Jennifer M Chan; Amy Weisman; Alex King; Susan Maksomski; Carrissa Shotwell; Claire Bailie; Helen Weaver; Rebecca Bodan; Estrella Guerrero; Matija Zmazek; Phuong Khuu
Journal:  Orphanet J Rare Dis       Date:  2019-06-07       Impact factor: 4.123

6.  Epidermolysis Bullosa in children: the central role of the pediatrician.

Authors:  Maria Rosaria Marchili; Giulia Spina; Marco Roversi; Cristina Mascolo; Elisabetta Pentimalli; Marialuisa Corbeddu; Andrea Diociaiuti; Maya El Hachem; Alberto Villani
Journal:  Orphanet J Rare Dis       Date:  2022-04-04       Impact factor: 4.123

7.  Prioritization of therapy uncertainties in Dystrophic Epidermolysis Bullosa: where should research direct to? an example of priority setting partnership in very rare disorders.

Authors:  Paula Davila-Seijo; Angela Hernández-Martín; Evanina Morcillo-Makow; Raúl de Lucas; Esther Domínguez; Natividad Romero; Eva Monrós; Marta Feito; Luis Carretero; Bea Aranegui; Ignacio García-Doval
Journal:  Orphanet J Rare Dis       Date:  2013-04-22       Impact factor: 4.123

Review 8.  Multicentre consensus recommendations for skin care in inherited epidermolysis bullosa.

Authors:  May El Hachem; Giovanna Zambruno; Eva Bourdon-Lanoy; Annalisa Ciasulli; Christiane Buisson; Smail Hadj-Rabia; Andrea Diociaiuti; Carolina F Gouveia; Angela Hernández-Martín; Raul de Lucas Laguna; Mateja Dolenc-Voljč; Gianluca Tadini; Guglielmo Salvatori; Cristiana De Ranieri; Stephanie Leclerc-Mercier; Christine Bodemer
Journal:  Orphanet J Rare Dis       Date:  2014-05-20       Impact factor: 4.123

  8 in total

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