Genetic Anomalies of Growth Hormone Deficiency in Pediatrics

被引:2
|
作者
Firouzi, Majid [1 ]
Sherkatolabbasieh, Hamidreza [1 ]
Shafizadeh, Shiva [2 ]
机构
[1] Lorestan Univ Med Sci, Fac Med, Dept Pediat, Khorramabad, Iran
[2] Lorestan Univ Med Sci, Dept Internal Med, Khorramabad, Iran
关键词
Hormone deficiency; growth hormone; genetic defects; pediatrics; pituitary disease; genetic anomalies; RECEPTOR GENE; HYPOGONADOTROPIC HYPOGONADISM; FUNCTIONAL-CHARACTERIZATION; OTX2; MUTATION; GH DEFICIENCY; SOX2; SHORT STATURE; PITUITARY; POU1F1; PROP1;
D O I
10.2174/1871530320666200704144912
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Several different proteins regulate, directly or indirectly, the production of growth hormones from the pituitary gland, thereby complex genetics is involved. Defects in these genes are related to the deficiency of growth hormones solely, or deficiency of other hormones, secreted from the pituitary gland including growth hormones. These studies can aid clinicians to trace the pattern of the disease between the families, start early treatment and predict possible future consequences. This paper highlights some of the most common and novel genetic anomalies concerning growth hormones, which are responsible for various genetic defects in isolated growth and combined pituitary hormone deficiency disease.
引用
收藏
页码:288 / 297
页数:10
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