Literature review, report, and analysis of genotype and clinical phenotype of a rare case of ulnar-mammary syndrome

OBJECTIVE: The clinical characteristics of Ulnar-mammary syndrome (UMS) caused by mutations in TBX3 (T-Box transcription factor 3) were studied and the correlation between genotype and clinical phenotype were analyzed to improve awareness and early diagnosis of the disease. METHODS: The clinical dat...

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Detalles Bibliográficos
Autores principales: Zhang, Xiwen, Chen, Lifen, Li, Lin, An, Jingjing, He, Qinyu, Zhang, Xuelei, Lu, Wenli, Xiao, Yuan, Dong, Zhiya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020526/
https://www.ncbi.nlm.nih.gov/pubmed/36937985
http://dx.doi.org/10.3389/fped.2023.1052931

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020526/
https://www.ncbi.nlm.nih.gov/pubmed/36937985
http://dx.doi.org/10.3389/fped.2023.1052931

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