<scp>STK4</scp> deficiency and epidermodysplasia verruciformis‐like lesions: A case report-Reference-Cited by-同舟云学术

STK4 deficiency and epidermodysplasia verruciformis‐like lesions: A case report

Published:2023-07-29 Issue:1 Volume:41 Page:96-99
ISSN:0736-8046
Container-title:Pediatric Dermatology
language:en
Short-container-title:Pediatric Dermatology

Author:

Gutierrez‐Marin Paula A.¹,Castano‐Jaramillo Lina M.²^ORCID,Velez‐Tirado Natalia²^ORCID,Villamil‐Osorio Milena³,Patiño Esteban⁴,Reina Maria Fernanda⁵,Hernandez Maribel Trujillo⁶^ORCID

Affiliation:

1. Department of Dermatology Universidad Militar Nueva Granada Bogota Colombia

2. Department of Pediatric Clinical Immunology HOMI Fundacion Hospital Pediatrico la Misericordia Bogota Colombia

3. Department of Pediatric Pulmonology HOMI Fundacion Hospital Pediatrico la Misericordia Bogota Colombia

4. Department of Pathology HOMI Fundacion Hospital Pediatrico la Misericordia Bogota Colombia

5. Department of Pediatric Rheumatology HOMI Fundacion Hospital Pediatrico la Misericordia Bogota Colombia

6. Department of Pediatric Dermatology HOMI Fundacion Hospital Pediatrico la Misericordia Bogota Colombia

Abstract

AbstractSerine/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.

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pde.15400

Reference10 articles.

1. Diversity in Serine/Threonine Protein Kinase-4 Deficiency and Review of the Literature

2. Inherited MST1 Deficiency Underlies Susceptibility to EV-HPV Infections