Work

ROSAH syndrome lacking splenomegaly and complete anhidrosis

Year: 2026

Type: article

Study design: Case Report

Source: BMJ Case Reports

DOI: 10.1136/bcr-2025-270922

Authors: Luiza De Gregori Dutra, Gisandra de Fátima Stangherlin, Heloísa Chiarini, Natalia Alini Haubenthal, Maria Luiza Vargas, Laryssa Huryn, Wadih M Zein, Kelly de Oliveira Harada, Liliani Mathias Brum, Christina Torres Kozycki

Institutions: Universidade Franciscana, Universidade Estadual de Londrina, National Eye Institute, National Institute of Allergy and Infectious Diseases

Language: English

Topic: Inflammasome and immune disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: National Institutes of Health

OpenAlex ID: W7128039936

FWCI: 1.822

Cites: 6

Cited by: 1

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