Abstracts tagged "Idiopathic Inflammatory Myopathies (IIM) and juvenile dermatomyositis"

Abstract Number: 396 • 2019 ACR/ARP Annual Meeting
Clinical Manifestations and Comparison of Subtypes of Juvenile Idiopathic Inflamatory Myopathies: Data from the REMICAM Registry
Jesús Loarce-Martos¹, Carmen Larena ², M. Ángeles Blázquez ¹, Beatriz Joven-Ibáñez ³, Patricia Carreira ³, Julia Martinez Barrio ⁴, Francisco javier López-Longo ⁵, Juan Carlos Lopez-Robledillo ⁶, Raquel Almodovar-Gonzalez ⁷, Irene Llorente ⁸, Eva Tomero-Muriel ⁸, Paloma García-De La Peña ⁹, Henry Moruno ¹⁰, Ana Pérez-Gómez ¹¹, Tatiana Cobo-Ibáñez ¹², María Jesús García De Yébenes ¹³ and Laura Nuño ¹⁴, ¹Hospital Universitario Ramón y Cajal, Madrid, Spain, ²Hospital Universitario Ramón y Cajal, Madrid, Madrid, Spain, ³Hospital Universitario 12 de Octubre, Madrid, Spain, ⁴Hospital Universitario Gregorio Marañón, Madrid, Spain, ⁵Hospital Universitario Gregorio Marañón, Madrid, ⁶Hospital Niño Jesús, Madrid, Spain, ⁷Hospital Universitario Fundación Alcorcón, Madrid, Spain, ⁸Hospital Universitario La Princesa, Madrid, Spain, ⁹Hospital HM San Chinarro, Madrid, Spain, ¹⁰Hospital Universitario Príncipe de Asturias, Madrid, ¹¹Hospital Universitario Príncipe de Asturias, Alcalá de Henares, Madrid, Spain, ¹²Hospital Universitario Infanta Sofía, Madrid, ¹³Instituto de Salud Musculoesquelética - Inmusc., Madrid, Spain, ¹⁴Hospital Universitario La Paz, Madrid
Background/Purpose: Juvenile idiopathic inflammatory myopathies (JIIM) are a heterogeneous group of autoimmune diseases affecting children, characterized by symmetric muscular weakness, cutaneous rash and systemic organ…

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