[A case of X-linked Alport syndrome with esophageal leiomyomatosis].

Tang, Z L; Yao, J; Zhang, P; He, X; Jia, L L; Shi, K L; Xia, Z K; Gao, C L

Tang, Z L; Yao, J; Zhang, P; He, X; Jia, L L; Shi, K L; Xia, Z K; Gao, C L.

Afiliação

Tang ZL; Department of Pediatrics, Jinling School of Clinical Medicine, Nanjing Medical University, Nanjing 210002, China.
Yao J; Department of Pediatrics, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210002, China.
Zhang P; Department of Pediatrics, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210002, China.
He X; Department of Pediatrics, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210002, China.
Jia LL; Department of Pediatrics, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210002, China.
Shi KL; Department of Pediatrics, Jinling School of Clinical Medicine, Nanjing Medical University, Nanjing 210002, China.
Xia ZK; Department of Pediatrics, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210002, China.
Gao CL; Department of Pediatrics, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210002, China.

Zhonghua Er Ke Za Zhi ; 62(3): 275-277, 2024 Mar 02.

Article em Zh | MEDLINE | ID: mdl-38378292

Assuntos

Leiomiomatose; Nefrite Hereditária; Humanos; Leiomiomatose/genética; Nefrite Hereditária/complicações; Nefrite Hereditária/genética

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leiomiomatose / Nefrite Hereditária Limite: Humans Idioma: Zh Revista: Zhonghua Er Ke Za Zhi Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: China

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