Central hypocortisolism as part of combined pituitary hormone deficiency due to mutations of PROP-1 gene

European Journal of Endocrinology

Volumn 143, Issue 3, 2000, Pages 347-352

  Asteria, C ^a   Oliveira, J H A ^a   Abucham, J ^a   Beck Peccoz, P ^a  

^a UNIVERSITY OF MILAN   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOTROPIN; FOLLITROPIN; GROWTH HORMONE; HYDROCORTISONE; HYPOPHYSIS HORMONE; LIOTHYRONINE; LUTEINIZING HORMONE; PROLACTIN; THYROTROPIN; THYROXINE; TRANSCRIPTION FACTOR PIT 1;

ADOLESCENT; ARTICLE; CLINICAL FEATURE; CORTICOTROPIN BLOOD LEVEL; FEMALE; FOLLITROPIN BLOOD LEVEL; FREE THYROXINE INDEX; GENE INACTIVATION; GENE MUTATION; GENE SEQUENCE; GROWTH HORMONE BLOOD LEVEL; GROWTH RETARDATION; HORMONE DEFICIENCY; HUMAN; HYDROCORTISONE BLOOD LEVEL; HYPOGONADISM; HYPOPHYSIS; HYPOTHALAMUS HYPOPHYSIS ADRENAL SYSTEM; HYPOTHYROIDISM; INSULIN TOLERANCE TEST; LIOTHYRONINE BLOOD LEVEL; LUTEINIZING HORMONE BLOOD LEVEL; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROLACTIN BLOOD LEVEL; THYROTROPIN BLOOD LEVEL;

EID: 0033794762     PISSN: 08044643     EISSN: None     Source Type: Journal    
DOI: 10.1530/eje.0.1430347     Document Type: Article

References (26)

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5. A tissue-specific transcription factor containing a homeodomain specifies a pituitary phenotype
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7. The Ames dwarf gene is required for Pit-1 gene activation
8. Pituitary lineage determination by Prophet of Pit-1 homeodomain factor defective in Ames dwarfism
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11. Mutations in the Pit-1 gene in children with combined pituitary hormone deficiency
12. Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene
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18. The PROP1 2- base pair deletion is a common cause of combined pituitary hormone deficiency
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26. Variable biological activity of thyroid-stimulating hormone