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

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: an enlarge...

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Veröffentlicht in:American Journal of Neuroradiology 2007-08, Vol.28 (7), p.1369-1370
Hauptverfasser: do Amaral, L.L.F, Ferreira, R.M, Ferreira, N.P.F.D, Mendonca, R.A, Marussi, V.H.R, da Cunha, J.L, Macaranduba, B.R, Medeiros, J.D
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Sprache:eng
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Zusammenfassung: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: an enlarged adenohypophysis, with striking hypointensity on T2-weighted images and slight hyperintensity on T1-weighted images. In one of the children, the follow-up MR imaging obtained 3 years after hormonal replacement revealed a decrease in the size of the anterior pituitary lobe.
ISSN:0195-6108
1936-959X
1432-1920
DOI:10.3174/ajnr.A0545