Short Stature Associated with Polymorphisms in Chromosome 1qh+, and 16qh+.
- Author:
Ki Hwan KIM
1
;
Sun Woo LEE
;
Myung Guan KIM
;
Duk Hee KIM
;
Ho Seong KIM
Author Information
1. Department of Pediatrics, College of Medicine, Yonsei University, Seoul, Korea. kimho@yumc.yonsei.ac.kr
- Publication Type:Case Report
- Keywords:
Short stature;
Chromosomal polymorphism;
Heterochromatin;
1qh+;
16qh+
- MeSH:
Child;
Chromosomes, Human, Pair 1;
Heterochromatin;
Humans
- From:Journal of Korean Society of Pediatric Endocrinology
2005;10(1):95-99
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Chromosomal polymorphism of constitutive heterochromatin regions of chromosome 1, 9, 16, and Y is a stable evolutionary feature that is thought to cause no phenotypic alterations. The presence of definite ethinic and age-related peculiarities of chromosomal polymorphism variants was established. Some authors reported the relationship of the separate variants with the phenotypic characteristics, such as reproductive function, physiological and anthropometric indices, and oncological diseases. Nevertheless, the role of constitutive heterochromatin is still unknown. We experienced and reported short children associated with polymorphisms in chromosme 1qh+ and 16qh+.
