A Case of Klinefelter Syndrome Differentially Diagnosed as a Cause of Gigantism.
- Author:
Joo Young KIM
1
;
Yong Jun CHOI
;
Sang Youl RHEE
Author Information
1. Department of Internal Medicine, Dongsuwon General Hospital, Suwon, Korea.
- Publication Type:Case Report
- Keywords:
Klinefelter syndrome;
Gigantism;
Hypogonadism;
Chromosomal disorders
- MeSH:
Atrophy;
Chromosome Disorders;
Comorbidity;
Gigantism;
Humans;
Hypogonadism;
Infertility;
Karyotype;
Klinefelter Syndrome;
Male;
Mass Screening;
Physical Examination;
X Chromosome;
Young Adult
- From:Korean Journal of Medicine
2011;80(3):343-347
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Klinefelter syndrome is a congenital disease that is associated with the existence of an extra X chromosome, and is one of the most common causes of male primary hypogonadism. In addition to hypogonadism-associated manifestations such as testicular atrophy and infertility, it is also well known that this syndrome may be associated with other systemic comorbidities. In this report, we describe a typical case of Klinefelter syndrome that was differentially diagnosed as a cause of gigantism. A 20-year-old male was admitted to evaluate the cause of tall stature. His height was 193.4 cm, and all screening tests for gigantism were negative. Physical examination revealed no clear evidence of secondary sexual characteristics, and the results of a hormonal assay were highly suspicious for primary hypogonadism. Based on these findings, we performed a chromosomal analysis and confirmed Klinefelter syndrome with a 47, XXY karyotype.
