Case report of severe refractory inflammatory dermatoses in a young female diagnosed with hereditary alpha tryptasemia

Hereditary alpha tryptasemia (HaT), an autosomal dominant condition first described in 2014, has previously been associated with multiple dermatologic, allergic, gastrointestinal, neuropsychiatric, autonomic, and connective tissue abnormalities. We describe a pediatric patient with predominantly mix...

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