Recombinant Growth hormone response in Indian girls with Turner syndrome

<p>Turner syndrome (TS) is characterized by short statute and ovarian dysgenesis in females with one X chromosome and partial or complete absence of the second X. It has an estimated birth prevalence of 1/2000 to 1/5000 female live births [1]. There is a global growth delay in TS characterized...

Full description

Saved in:
Bibliographic Details
Main Authors: Inderpal Singh Kochar (Author), Smita Ramachandran (Author), Aashish Sethi (Author)
Format: Book
Published: International Journal of Clinical Endocrinology and Metabolism - Peertechz Publications, 2018-10-29.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 peertech__10_17352_ijcem_000029
042 |a dc 
100 1 0 |a Inderpal Singh Kochar  |e author 
700 1 0 |a  Smita Ramachandran  |e author 
700 1 0 |a Aashish Sethi  |e author 
245 0 0 |a Recombinant Growth hormone response in Indian girls with Turner syndrome 
260 |b International Journal of Clinical Endocrinology and Metabolism - Peertechz Publications,   |c 2018-10-29. 
520 |a <p>Turner syndrome (TS) is characterized by short statute and ovarian dysgenesis in females with one X chromosome and partial or complete absence of the second X. It has an estimated birth prevalence of 1/2000 to 1/5000 female live births [1]. There is a global growth delay in TS characterized by slight intrauterine growth retardation, delayed growth during infancy and childhood, and lack of a pubertal growth spurt [2].</p> 
540 |a Copyright © Inderpal Singh Kochar et al. 
546 |a en 
655 7 |a Research Article  |2 local 
856 4 1 |u https://doi.org/10.17352/ijcem.000029  |z Connect to this object online.