Marshall syndrome

A malformation syndrome that is characterized by facial dysmorphism, severe hypoplasia of the nasal bones and frontal sinuses, ocular involvement, early-onset hearing loss, skeletal and anhidrotic ectodermal anomalies and short stature with spondyloepiphyseal dysplasia and early-onset osteoarthritis.

Pharyngitis

Inflammation (due to infection or irritation) of the pharynx.


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PMID (PMCID)
27858841
(5591089)
 FEMALE
Marshall syndrome in a young child, a reality: Case report.
Trandafir LM, Chiriac MI, Diaconescu S, Ioniuc I, Miron I, Rusu D.
Medicine (Baltimore). 2016;95(44):e5065.
Recurrent fever syndrome, known as the Marshall syndrome (MS), is a clinical entity that includes several clinical features, such as: fever (39-40C) that occurs repeatedly at variable intervals (3-8 weeks) and in episodes of 3 to 6 days, cervical adenopathy, pharyngitis, and aphthous stomatitis.