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Published in: Endocrine 3/2015

01-08-2015 | Endocrine Imaging

Pituitary stalk interruption and olfactory bulbs aplasia/hypoplasia in a man with Kallmann syndrome and reversible gonadotrope and somatotrope deficiencies

Authors: Julie Sarfati, Alexandru Saveanu, Jacques Young

Published in: Endocrine | Issue 3/2015

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Excerpt

Kallmann syndrome (KS) is characterized by congenital hypogonadotropic hypogonadism (CHH) and anosmia/hyposmia related to aplasia/hypoplasia of the olfactory bulbs (OB) [1]. In KS, the gonadotropin deficiency is isolated, the statural growth is preserved and other pituitary functions, particularly growth hormone (GH) secretion are normal, as well as hypothalamo-pituitary morphology [2]. …
Literature
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go back to reference L. Maione, S. Benadjaoud, C. Eloit et al., Computed tomography of the anterior skull base in Kallmann syndrome reveals specific ethmoid bone abnormalities associated with olfactory bulb defects. J. Clin. Endocrinol. Metab. 98, E537–E546 (2013)PubMedCrossRef L. Maione, S. Benadjaoud, C. Eloit et al., Computed tomography of the anterior skull base in Kallmann syndrome reveals specific ethmoid bone abnormalities associated with olfactory bulb defects. J. Clin. Endocrinol. Metab. 98, E537–E546 (2013)PubMedCrossRef
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go back to reference J. Young, Approach to the male patient with congenital hypogonadotropic hypogonadism. J. Clin. Endocrinol. Metab. 97, 707–718 (2012)PubMedCrossRef J. Young, Approach to the male patient with congenital hypogonadotropic hypogonadism. J. Clin. Endocrinol. Metab. 97, 707–718 (2012)PubMedCrossRef
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go back to reference T. Raivio, M. Avbelj, M.J. McCabe et al., Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia. J. Clin. Endocrinol. Metab. 97, E694–E699 (2012)PubMedCentralPubMedCrossRef T. Raivio, M. Avbelj, M.J. McCabe et al., Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia. J. Clin. Endocrinol. Metab. 97, E694–E699 (2012)PubMedCentralPubMedCrossRef
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go back to reference R. Reynaud, F. Albarel, A. Saveanu et al., Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms. Eur. J. Endocrinol. 164, 457–465 (2011) R. Reynaud, F. Albarel, A. Saveanu et al., Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms. Eur. J. Endocrinol. 164, 457–465 (2011)
Metadata
Title
Pituitary stalk interruption and olfactory bulbs aplasia/hypoplasia in a man with Kallmann syndrome and reversible gonadotrope and somatotrope deficiencies
Authors
Julie Sarfati
Alexandru Saveanu
Jacques Young
Publication date
01-08-2015
Publisher
Springer US
Published in
Endocrine / Issue 3/2015
Print ISSN: 1355-008X
Electronic ISSN: 1559-0100
DOI
https://doi.org/10.1007/s12020-014-0475-8

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