In:
JMS SKIMS, Sheri-i-Kashmir Institute of Medical Sciences, Vol. 20, No. 2 ( 2017-12-09), p. 104-106
Abstract:
Background : Laron & colleagues (1966) reported a rare genetic disorder in Israliei Jewish sublings which was characterized by insensitivity to growth hormone due to abnormality in growth hormone receptor or post receptor signaling pathway.Case Report: We hereby report a case of a 5 year old female child who presented to us with features similar to Laron syndrome. The diagnosis was made & confirmed by various Lab. investigations like low IGF-I levels and managed accordingly. JMS 2017; 20 (2):104-106
Type of Medium:
Online Resource
ISSN:
0972-110X
,
0972-110X
DOI:
10.33883/jms.v20i2.204
Language:
Unknown
Publisher:
Sheri-i-Kashmir Institute of Medical Sciences
Publication Date:
2017
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