Congenital hypopituitarism in two brothers with a duplication of the ‘acrogigantism gene’ GPR101: clinical findings and review of the literature

PURPOSE: Congenital hypopituitarism (CH) can cause significant morbidity or even mortality. In the majority of patients, the etiology of CH is unknown. Understanding the etiology of CH is important for anticipation of clinical problems and for genetic counselling. Our previous studies showed that on...

Descripción completa

Detalles Bibliográficos
Autores principales: Elizabeth, Melitza S. M., Verkerk, Annemieke J. M. H., Hokken-Koelega, Anita C. S., Verlouw, Joost A. M., Argente, Jesús, Pfaeffle, Roland, Neggers, Sebastian J. C. M. M., Visser, Jenny A., de Graaff, Laura C. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966638/
https://www.ncbi.nlm.nih.gov/pubmed/33184694
http://dx.doi.org/10.1007/s11102-020-01101-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966638/
https://www.ncbi.nlm.nih.gov/pubmed/33184694
http://dx.doi.org/10.1007/s11102-020-01101-8

Ejemplares similares