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Combined Pituitary Hormone Deficiency and PROP-1 Mutation in Two Siblings: A Distinct MR Imaging Pattern of Pituitary Enlargement

SUMMARY: Mutations of the PROP-1 gene are the most frequent genetic defect in patients with combined pituitary hormone insufficiency. We present the cases of 2 siblings with PROP-1 mutations whom we observed longitudinally. Their initial pituitary MR imaging examinations showed identical findings: a...

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Bibliografski detalji
Izdano u:AJNR Am J Neuroradiol
Glavni autori: do Amaral, L.L.F., Ferreira, R.M., Ferreira, N.P.F.D., Mendonça, R.A., Marussi, V.H.R., da Cunha, J.L., Maçaranduba, B.R., Medeiros, J.D.
Format: Artigo
Jezik:Inglês
Izdano: American Society of Neuroradiology 2007
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7977640/
https://ncbi.nlm.nih.gov/pubmed/17698542
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3174/ajnr.A0545
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