Mowat-Wilson Syndrome Presenting With Purpura Fulminans.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 30573661.
- Also identified by DOI 10.1542/peds.2018-0922.
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Abstract
Purpura fulminans is a rapidly progressive syndrome of intravascular thrombosis and hemorrhagic infarction of the skin. The most common infectious etiology is <i>Neisseria meningitidis</i> sepsis, and less commonly it has been documented as a complication of invasive <i>Streptococcus pneumoniae</i> 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.
Medical subject headings
- Hirschsprung Disease
- Intellectual Disability
- Microcephaly
- Pneumococcal Infections
- Purpura Fulminans
- Streptococcus pneumoniae