Please use this identifier to cite or link to this item: 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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