Literature DB >> 27386970

Advancement in management of epidermolysis bullosa.

Heather I Cohn1, Joyce M C Teng.   

Abstract

PURPOSE OF REVIEW: Epidermolysis bullosa is a hereditary skin disorder characterized by skin fragility. However, the disease can manifest in many different organ systems, therefore children born with epidermolysis bullosa may have life long, complex medical needs. In this review, we will use a system-based approach to highlight important aspects of disease management and recent advancements in each of the areas. In addition, we will overview some of the cutting edge therapeutic developments in epidermolysis bullosa. RECENT
FINDINGS: Recent advancements in supportive care of epidermolysis bullosa with focus on wound, pain, pruritus and nutrition status were discussed. Clinical surveillance and complication prevention are critical to improve clinical outcomes. Generalized epidermolysis bullosa is a systemic disease with increased morbidity and mortality; therefore, complex care using a multidisciplinary approach will provide the greatest benefits for patients. Current targeted treatments for epidermolysis bullosa aim at restoring the skin integrity using protein, cell, and gene therapies.
SUMMARY: Improvement in care of epidermolysis bullosa in recent years results from keen clinical observation, novel molecular targeting, and the embracement of translational research.

Entities:  

Mesh:

Year:  2016        PMID: 27386970     DOI: 10.1097/MOP.0000000000000380

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  6 in total

1.  Surgical management of squamous cell carcinoma arising in patients affected by epidermolysis bullosa: a comparative study.

Authors:  Alessia Paganelli; Camilla Reggiani; Chiara Fiorentini; Mario Lando; Anna M Cesinaro; Cristina Magnoni
Journal:  Int Wound J       Date:  2020-01-15       Impact factor: 3.315

2.  Is Cannabis Legalization Eliciting Abusive Behaviors in Parents? A Case Report.

Authors:  Marianna Russo; Donata Favretto; Stefano Sartori; Paola Facchin; Melissa Rosa-Rizzotto
Journal:  J Pediatr Pharmacol Ther       Date:  2022-07-06

3.  BP180 dysfunction triggers spontaneous skin inflammation in mice.

Authors:  Yang Zhang; Bin-Jin Hwang; Zhen Liu; Ning Li; Kendall Lough; Scott E Williams; Jinbo Chen; Susan W Burette; Luis A Diaz; Maureen A Su; Shengxiang Xiao; Zhi Liu
Journal:  Proc Natl Acad Sci U S A       Date:  2018-06-04       Impact factor: 11.205

Review 4.  Dental-craniofacial manifestation and treatment of rare diseases.

Authors:  En Luo; Hanghang Liu; Qiucheng Zhao; Bing Shi; Qianming Chen
Journal:  Int J Oral Sci       Date:  2019-02-20       Impact factor: 6.344

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

  6 in total

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