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Pediatr Dermatol ; 41(1): 96-99, 2024.
Article in English | MEDLINE | ID: mdl-37515487

ABSTRACT

Serine/threonine kinase 4 deficiency (STK4 or MST1, OMIM:614868) is an autosomal recessive (AR) combined immunodeficiency that can present with skin lesions such as epidermodysplasia verruciformis-like lesions (EVLL). Herein, we describe a 17-year-old male patient born from consanguineous parents presenting with recurrent respiratory infections, verruciform plaques, poikiloderma, chronic benign lymphoproliferation, and Sjögren syndrome with suspected interstitial lymphocytic pneumonia.


Subject(s)
Epidermodysplasia Verruciformis , Primary Immunodeficiency Diseases , Skin Diseases , Male , Humans , Adolescent , Epidermodysplasia Verruciformis/diagnosis , Epidermodysplasia Verruciformis/genetics , Epidermodysplasia Verruciformis/pathology , Papillomaviridae , Primary Immunodeficiency Diseases/diagnosis , Protein Serine-Threonine Kinases , Intracellular Signaling Peptides and Proteins
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