About a Suggestive Association Between Fanconi Anemia and Laron Syndrome

2018 ◽  
Vol 355 (6) ◽  
pp. 615-616
Author(s):  
I. Castilla-Cortazar ◽  
G.A. Aguirre ◽  
J.R. De Ita
2017 ◽  
Vol 353 (5) ◽  
pp. 425-432 ◽  
Author(s):  
Inma Castilla-Cortazar ◽  
Julieta Rodriguez de Ita ◽  
Gabriel Amador Aguirre ◽  
Fabiola Castorena-Torres ◽  
Jesús Ortiz-Urbina ◽  
...  

2018 ◽  
Vol 355 (6) ◽  
pp. 614-615
Author(s):  
Benilde García-de Teresa ◽  
Sara Frias

2015 ◽  
Vol 21 ◽  
pp. 166-167
Author(s):  
Anirban Sinha ◽  
Ravindra Shukla ◽  
Biplab Mandal ◽  
Asish Basu ◽  
Satyam Chakraborty ◽  
...  

JMS SKIMS ◽  
2017 ◽  
Vol 20 (2) ◽  
pp. 104-106
Author(s):  
Javaid Ahmad Bhat ◽  
Moomin Hussain Bhat ◽  
Hilal Bhat ◽  
Mona Sood ◽  
Shariq Rashid Masoodi

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  


2006 ◽  
Vol 26 (1) ◽  
pp. 81-96 ◽  
Author(s):  
Sara R. Fagerlie ◽  
Grover C. Bagby

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