MeSH Browser

MeSH Supplementary: Combined Pituitary Hormone Deficiency
Unique ID: C580003
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C580003
Entry Term(s): Panhypopituitarism
Registry Number: 0
Heading Mapped to: *Hypopituitarism
Frequency: 305
Note: A hereditary autosomal recessive form of hypopituitarism that is characterized by growth retardation, HYPOTHYROIDISM, reduced levels of CORTISOL, and absent or DELAYED PUBERTY due to low levels of LUTEINIZING HORMONE or FOLLICLE-STIMULATING HORMONE . Rarely, INTELLECTUAL DISABILITY, neck abnormalities, and OPTIC NERVE defects may also occur. Mutations in the PROP1 gene have been identified in some cases. OMIM: 262600
Date of Entry: 2013/10/24
Revision Date: 2015/08/18

Combined Pituitary Hormone Deficiency MeSH Supplementary Concept Data 2024