Literature DB >> 30573661

Mowat-Wilson Syndrome Presenting With Purpura Fulminans.

Claudia G Nevarez Flores1, Alexander P Sun2, Howard Hast3.   

Abstract

Purpura fulminans is a rapidly progressive syndrome of intravascular thrombosis and hemorrhagic infarction of the skin. The most common infectious etiology is Neisseria meningitidis sepsis, and less commonly it has been documented as a complication of invasive Streptococcus pneumoniae In children who are otherwise healthy, splenic dysfunction is a significant predisposing factor for invasive pneumococcal infection. We present the case of a 10-month-old girl with a history of developmental delay, who developed an overwhelming infection complicated by purpura fulminans and was found to have previously undiagnosed Mowat-Wilson syndrome with anatomic asplenia. We propose screening patients with clinical features suggestive of Mowat-Wilson syndrome for asplenia to evaluate the need for additional preventive care.
Copyright © 2019 by the American Academy of Pediatrics.

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Year:  2019        PMID: 30573661     DOI: 10.1542/peds.2018-0922

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  2 in total

1.  The Role of ZEB2 in Human CD8 T Lymphocytes: Clinical and Cellular Immune Profiling in Mowat-Wilson Syndrome.

Authors:  Katie Frith; C Mee Ling Munier; Lucy Hastings; David Mowat; Meredith Wilson; Nabila Seddiki; Rebecca Macintosh; Anthony D Kelleher; Paul Gray; John James Zaunders
Journal:  Int J Mol Sci       Date:  2021-05-18       Impact factor: 5.923

2.  A novel nonsense mutation of ZEB2 gene in a Chinese patient with Mowat-Wilson syndrome.

Authors:  Yuan Hu; Qi Peng; Keze Ma; Siping Li; Chunbao Rao; Baimao Zhong; Xiaomei Lu
Journal:  J Clin Lab Anal       Date:  2020-06-10       Impact factor: 2.352

  2 in total

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