Suprasellar mass mimicking a hypothalamic glioma in a patient with a complete PROP1 deletion

Author:

Akcay Arzu,Ulucan Korkut,Taskin Necati,Boyraz Mehmet,Akcay Teoman,Zurita Olga,Gomez Ana,Heath Karen E.,Campos-Barros Angel

Funder

Fondo de Investigación Sanitaria, ISCIII, Ministerio de Economía y Competividad, Spain

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference16 articles.

1. Pituitary gland development: an update;Bancalari;Endocr. Dev.,2012

2. Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia;Raivio;J. Clin. Endocrinol. Metab.,2012

3. Genetic screening of combined pituitary hormone deficiency: experience in 195 patients;Reynaud;J. Clin. Endocrinol. Metab.,2006

4. Genetic screening in a cohort of 2030 patients with congenital hypopituitarism: current knowledge and future directions;Alatzoglou;Endocr. Rev.,2012

5. Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion;Abrao;Clin. Endocrinol. (Oxf.),2006

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