Clinical case
Familial combined pituitary hormone deficiency by a mutation in PROP1: 4 of 7 brothers affected
Panhipopituitarismo familiar por mutação do gene PROP1: 4 de 7 irmãos afectados
Eva Laua,
, Paula Freitasa, Eduarda Coutinhob, Manuel Carlos Lemosb, Davide Carvalhoa
Corresponding author
a Department of Endocrinology, Diabetes and Metabolism, Centro Hospitalar São João; Faculty of Medicine University of Porto; Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal
b Health Sciences Research Centre (CICS), Faculty of Health Sciences, University of Beira Interior, Covilhã, Portugal
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