Combined pituitary hormone deficiency: current and future status

Over the last two decades, the understanding of the mechanisms involved in pituitary ontogenesis has largely increased. Since the first description of POU1F1 human mutations responsible for a well-defined phenotype without extra-pituitary malformation, several other genetic defects of transcription...

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Bibliographic Details
Published in:	Journal of endocrinological investigation Vol. 38; no. 1; pp. 1 - 12
Main Authors:	Castinetti, F., Reynaud, R., Quentien, M.-H., Jullien, N., Marquant, E., Rochette, C., Herman, J.-P., Saveanu, A., Barlier, A., Enjalbert, A., Brue, T.
Format:	Journal Article
Language:	English
Published:	Cham Springer International Publishing 01.01.2015
Subjects:	Animals Endocrinology Forecasting Humans Hypopituitarism - diagnosis Hypopituitarism - etiology Hypopituitarism - genetics Medicine Medicine & Public Health Metabolic Diseases Mutation - genetics Phenotype Pituitary Gland - growth & development Pituitary Gland - secretion Pituitary Hormones - genetics Pituitary Hormones - secretion Review Corticotroph deficiency Pituitary development Gonadotroph deficiency Somatotroph deficiency Hypothalamus Transcription factor Thyrotroph deficiency
ISSN:	1720-8386, 1720-8386
Online Access:	Get full text
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