THU187 Genotype-Phenotype Correlation, Clinical Presentation And Feminizing Surgery In Children With Congenital Adrenal Hyperplasia Due To 21-Hydroxylase Deficiency: A Nationwide Multi-Center Study

Disclosure: M. Lind-Holst: None. A. Berglund: None. M. Duno: None. G. Hvistendahl: None. M. Fossum: None. A. Juul: None. N. Jørgensen: None. K.M. Main: None. C.H. Gravholt: None. D. Hansen: None. Background: Congenital adrenal hyperplasia (CAH) due to 21 hydroxylase deficiency (21OHD) is a common au...

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Detalles Bibliográficos
Autores principales: Lind-Holst, Marie, Berglund, Agnethe, Duno, Morten, Hvistendahl, Gitte, Fossum, Magdalena, Juul, Anders, Jørgensen, Niels, Main, Katharina Maria, Gravholt, Claus Hojbjerg, Hansen, Dorte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Pediatric Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10554250/
http://dx.doi.org/10.1210/jendso/bvad114.1438

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10554250/
http://dx.doi.org/10.1210/jendso/bvad114.1438

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