Publication:
A Case with Laron Syndrome

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Date
2019-07-01T00:00:00Z
Authors
ÖZGEN, İLKER TOLGA
CESUR, Yaşar
Kutlu, Esra
Yesil, Gozde
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Abstract
Laron syndrome (LS) is a rare disorder leading to short stature as a result of growth hormone (GH) insensitivity. It is caused by mutations in GH receptor gene and characterized by post-natal growth retardation, craniofacial abnormalities, high serum GH and low insulin-like growth factor-1 (IGF-I) levels. Several different genetic mutations have been documented up to date. In this article, a patient with LS is reported.
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ÖZGEN İ. T. , Kutlu E., CESUR Y., Yesil G., -A Case with Laron Syndrome-, BEZMIALEM SCIENCE, cilt.7, ss.251-254, 2019
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