Mutations and Pituitary Morphology in a Series of 82 Patients with PROP1 Gene Defects
Mutations and Pituitary Morphology in a Series of 82 Patients with PROP1 Gene Defects
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Publisher
Basel, Switzerland: S. Karger AG
Journal title
Language
English
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Publisher
Basel, Switzerland: S. Karger AG
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Scope and Contents
Contents
Background/Aims: Defects of the PROP1 gene are the most prevalent genetic cause of combined pituitary hormone deficiency. Previous observations in affected patients have shown pituitary size ranging from hypoplasia to overt pituitary mass and evolution of size over the lifespan. Methods: We evaluated pituitary size and morphology in PROP1-mutation...
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Full title
Mutations and Pituitary Morphology in a Series of 82 Patients with PROP1 Gene Defects
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Record Identifier
TN_cdi_proquest_miscellaneous_907035668
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_907035668
Other Identifiers
ISSN
1663-2818
E-ISSN
1663-2826
DOI
10.1159/000332693
