Juvenile Clinically Amyopathic Dermatomyositis: A Case Report and Review of Literature
Identifieur interne : 000822 ( Ncbi/Curation ); précédent : 000821; suivant : 000823Juvenile Clinically Amyopathic Dermatomyositis: A Case Report and Review of Literature
Auteurs : Vadood Javadi Parvaneh [Iran] ; Mehrdad Yasaei [Iran] ; Khosro Rahmani [Iran] ; Yalda Nilipour [Iran]Source :
- Iranian Journal of Child Neurology [ 1735-4668 ] ; 2019.
Abstract
Juvenile clinically amyopathic dermatomyositis (juvenile CADM) is a rare rheumatologic disease in children defined as the presence of the hallmark cutaneous features of dermatomyositis in absence of muscle involvement
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PubMed: 31327976
PubMed Central: 6586448
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<author><name sortKey="Javadi Parvaneh, Vadood" sort="Javadi Parvaneh, Vadood" uniqKey="Javadi Parvaneh V" first="Vadood" last="Javadi Parvaneh">Vadood Javadi Parvaneh</name>
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<author><name sortKey="Yasaei, Mehrdad" sort="Yasaei, Mehrdad" uniqKey="Yasaei M" first="Mehrdad" last="Yasaei">Mehrdad Yasaei</name>
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<front><div type="abstract" xml:lang="en"><p>Juvenile clinically amyopathic dermatomyositis (juvenile CADM) is a rare rheumatologic disease in children defined as the presence of the hallmark cutaneous features of dermatomyositis in absence of muscle involvement<bold>. </bold>
In this article, we report an Iranian 14.5-year-old girl presented to Rheumatology Clinic of Mofid Children's Hospital, Tehran, Iran in Jan 2016 with cutaneous complaints diagnosed with juvenile CADM. Finally, we provide a literature review of previous studies on juvenile CADM.</p>
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