A patient with pseudohypoparathyroidism type 1A previously misdiagnosed as hereditary multiple exostosis: A case report.

Zhang, Jie; Guan, Ming; Zhao, Shiyong; Wu, Suling; Weng, Lingwei; Sheng, Wenbin

Zhang, Jie; Guan, Ming; Zhao, Shiyong; Wu, Suling; Weng, Lingwei; Sheng, Wenbin.

Afiliação

Zhang J; Department of Pediatrics, Hangzhou Children's Hospital, Hangzhou, Zhejiang 310014, P.R. China.
Guan M; Department of Otolaryngology, Affiliated Hangzhou First People's Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang 310006, P.R. China.
Zhao S; Department of Pediatrics, Hangzhou Children's Hospital, Hangzhou, Zhejiang 310014, P.R. China.
Wu S; Department of Pediatrics, Hangzhou Children's Hospital, Hangzhou, Zhejiang 310014, P.R. China.
Weng L; Department of Pediatrics, Hangzhou Children's Hospital, Hangzhou, Zhejiang 310014, P.R. China.
Sheng W; Department of Pediatrics, Hangzhou Children's Hospital, Hangzhou, Zhejiang 310014, P.R. China.

Exp Ther Med ; 24(3): 597, 2022 Sep.

Article em En | MEDLINE | ID: mdl-35949342

Palavras-chave

guanine nucleotide-binding protein α stimulating; hereditary multiple exostoses; pseudohypoparathyroidism type 1A

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Exp Ther Med Ano de publicação: 2022 Tipo de documento: Article