CINCA Syndrome With New NLRP3 Mutation and Unreported Complication of Thyroid Carcinoma

BACKGROUND: Chronic infantile neurologic cutaneous and articular syndrome (CINCA) is the most severe phenotype of cryopyrin-associated periodic syndromes (CAPS) and is caused by a missense mutation in NLRP3 gene. CASE PRESENTATION: We are reporting a 15-year-old male patient with complaints of chron...

Descripción completa

Detalles Bibliográficos
Autores principales: Salehzadeh, Farhad, Barak, Manuchehr, Hosseiniasl, Saied, Shahbazfar, Ehsan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557019/
https://www.ncbi.nlm.nih.gov/pubmed/31217698
http://dx.doi.org/10.1177/1179547619854705

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557019/
https://www.ncbi.nlm.nih.gov/pubmed/31217698
http://dx.doi.org/10.1177/1179547619854705

Ejemplares similares