Concomitant occurrence of Turner syndrome and growth hormone deficiency.
10.3345/kjp.2016.59.11.S121
- Author:
Jung YU
1
;
Ha Young SHIN
;
Chong Guk LEE
;
Jae Hyun KIM
Author Information
1. Department of Pediatrics, Inje University Ilsan Paik Hospital, Goyang, Korea. pedendo@paik.ac.kr
- Publication Type:Case Report
- Keywords:
Turner syndrome;
Growth hormone deficiency;
Short stature
- MeSH:
Chromosome Aberrations;
Female;
Growth Hormone*;
Humans;
Karyotype;
Karyotyping;
Korea;
Phenotype;
Physical Examination;
Pituitary Gland;
Prognosis;
Sex Chromosomes;
Turner Syndrome*
- From:Korean Journal of Pediatrics
2016;59(Suppl 1):S121-S124
- CountryRepublic of Korea
- Language:English
-
Abstract:
Turner syndrome (TS) is a genetic disorder in phenotypic females that has characteristic physical features and presents as partial or complete absence of the second sex chromosome. Growth hormone deficiency (GHD) is a condition caused by insufficient release of growth hormone from the pituitary gland. The concomitant occurrence of TS and GHD is rare and has not yet been reported in Korea. Here we report 2 cases of TS and GHD. In case 1, GHD was initially diagnosed. Karyotyping was performed because of the presence of the typical phenotype and poor response to growth hormone therapy, which revealed 45,X/45,X+mar. The patient showed increased growth velocity after the growth hormone dose was increased. In case 2, a growth hormone provocation test and chromosomal analysis were performed simultaneously because of decreased growth velocity and the typical TS phenotype, which showed GHD and a mosaic karyotype of 45,X/46,XX. The patient showed spontaneous pubertal development. In female patients with short stature, it is important to perform a throughout physical examination and test for hormonal and chromosomal abnormalities because diagnostic accuracy is important for treatment and prognosis.
