Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome: The First Familial Case in China and Novel Mutations of the Proteoglycan 4 Gene.

Zhang, Jun-Mei; Gao, Feng-Qiao; Li, Cai-Feng; Kuang, Wei-Ying; Deng, Jiang-Hong; Tan, Xiao-Hua; Li, Chao; Li, Shi-Peng

Zhang, Jun-Mei; Gao, Feng-Qiao; Li, Cai-Feng; Kuang, Wei-Ying; Deng, Jiang-Hong; Tan, Xiao-Hua; Li, Chao; Li, Shi-Peng.

Afiliação

Zhang JM; Department of Rheumatology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Gao FQ; Department of Rheumatology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Li CF; Department of Rheumatology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China. licaifeng123@yeah.net.
Kuang WY; Department of Rheumatology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Deng JH; Department of Rheumatology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Tan XH; Department of Rheumatology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Li C; Department of Rheumatology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Li SP; Department of Rheumatology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.

J Rheumatol ; 49(12): 1400-1402, 2022 12.

Article em En | MEDLINE | ID: mdl-36109080

Assuntos

Artropatia Neurogênica; Coxa Vara; Proteoglicanas; Humanos; Coxa Vara/genética; Mutação; Proteoglicanas/genética

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Artropatia Neurogênica / Proteoglicanas / Coxa Vara Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

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