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https://hdl.handle.net/11499/7334
Title: | A rare cause of short stature: transsphenoidal encephalocele | Authors: | Bayram, Özhan Ağladıoğlu Yılmaz, Sebahat Kadir, Ağladıoğlu Ali, Koçyiğit |
Keywords: | Growth hormone deficiency Short stature Transsphenoidal encephalocele clonidine growth hormone levodopa somatomedin binding protein 3 somatomedin C human growth hormone Article body height body weight bone age case report child encephalocele growth hormone deficiency human male physical examination priority journal provocation test school child short stature transsphenoidal encephalocele complication deficiency dwarfism metabolism Child Dwarfism Encephalocele Human Growth Hormone Humans Male |
Publisher: | Springer Verlag | Abstract: | Basal encephaloceles are rare, accounting for about 1.5 % of all encephaloceles. Transsphenoidal encephaloceles represent less than 5 % of basal encephaloceles. Respiratory and feeding difficulties due to mass effect in the oral or nasal cavity and episodes of recurrent meningitis are the main clinical features. Diagnosis is established in the first year of life, but without characteristic facies, the diagnosis can be delayed to adolescence or adulthood. We report the case of a 10-year-old boy who presented with short stature and eventually was diagnosed with a growth hormone deficiency because of mass effect of transsphenoidal encephalocele. Unusual presentation of an encephalocele as a short stature is described. © 2013, Springer-Verlag Berlin Heidelberg. | URI: | https://hdl.handle.net/11499/7334 https://doi.org/10.1007/s00431-013-2175-4 |
ISSN: | 0340-6199 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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