The natural history of the R120C PROP1 mutation reveals a wide phenotypic variability in two untreated adult brothers with combined pituitary hormone deficiency

Endocrine

Volumn 30, Issue 3, 2006, Pages 365-369

  Vieira, Teresa C ^a   Da Silva, Magnus R Dias ^a   Abucham, Julio ^a  

^a FEDERAL UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Combined pituitary hormone deficiency; Hypopituitarism; Mutation, PROP1; Pituitary transcription factors

Indexed keywords

TRANSCRIPTION FACTOR PIT 1;

ADULT; ARTICLE; BODY HEIGHT; CASE REPORT; DEVELOPMENT; DISEASE SEVERITY; FOLLOW UP; GENE MUTATION; GENETIC VARIABILITY; GENETICS; GROWTH HORMONE DEFICIENCY; HOMOZYGOSITY; HORMONE DEFICIENCY; HUMAN; HYPOGONADISM; HYPOPHYSIS; MALE; PHENOTYPE; PRIORITY JOURNAL;

EID: 34347348223     PISSN: 1355008X     EISSN: 15590100     Source Type: Journal    
DOI: 10.1007/s12020-006-0015-2     Document Type: Article

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