Coexistence of Growth Hormone Deficiency and Pituitary Microadenoma in a Child with Unique Mosaic Turner Syndrome: A Case Report and Literature Review

Turner syndrome (TS) is a genetic disorder with phenotypic heterogeneity caused by the monosomy or structural abnormalities of the X chromosome, and it has a prevalence of about 1/2500 females live birth. The variable clinical features of TS include short stature, gonadal failure, and skeletal dyspl...

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Detalles Bibliográficos
Autores principales: Park, Eu Gene, Kim, Eun-Jung, Kim, Eun-Jee, Kim, Hyun-Young, Kim, Sun-Hee, Yang, Aram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7600578/
https://www.ncbi.nlm.nih.gov/pubmed/33020433
http://dx.doi.org/10.3390/diagnostics10100783

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7600578/
https://www.ncbi.nlm.nih.gov/pubmed/33020433
http://dx.doi.org/10.3390/diagnostics10100783

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