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A Case with Laron Syndrome
Author(s) -
İlker Tolga Özgen,
Esra Kutlu,
Yaşar Cesur,
Gözde Yeşil
Publication year - 2019
Publication title -
bezmialem science
Language(s) - English
Resource type - Journals
ISSN - 2148-2373
DOI - 10.14235/bas.galenos.2018.2385
Subject(s) - medicine , pediatrics
Along with autosomal recessive inheritance, the Laron syndrome (LS) is a congenital disorder, which is infrequent in prevalence. The disease was firstly diagnosed by Laron et al. (1) on several oriental Jewish families in 1966. Clinically, post-natal growth retardation is observed in patients with this syndrome. Adult length of these patients remain between -4 and -10 SDS unless they receive necessary treatment (2).

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