Cargando…
The correlation between clinical features and ultrastructure of testis of non-mosaic Klinefelter's syndrome patients with hypogonadism and androgen deficiency: A case report
BACKGROUND: Klinefelter Syndrome (KS) is a sex chromosomal syndrome usually with an extra X chromosome (47, XXY) in males, which has various phenotype (mosaicism 47, XXY/46, XY, or more chromosomes 48, XXXY, 49, XXXXY) and clinical features, including eunuchoid body proportions, abnormally long legs...
Autores principales: | Zhang, Bin, Li, Fudong, Huang, Chuang, Xu, Liuting, Cao, Zhigang, Kang, Yafen, Jiang, Wei, Chang, Dehui |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10559353/ https://www.ncbi.nlm.nih.gov/pubmed/37809695 http://dx.doi.org/10.1016/j.heliyon.2023.e19940 |
Ejemplares similares
-
The role of hypogonadism in Klinefelter Syndrome
por: Høst, Christian, et al.
Publicado: (2014) -
Hypogonadism Makes Dyslipidemia in Klinefelter's Syndrome
por: Lee, Hyo Serk, et al.
Publicado: (2017) -
Klinefelter syndrome (KS): genetics, clinical phenotype and hypogonadism
por: Bonomi, M., et al.
Publicado: (2016) -
Reduced fibrin clot lysis in Klinefelter syndrome associated with hypogonadism
por: Chang, Simon, et al.
Publicado: (2022) -
Testis Transcriptome Modulation in Klinefelter Patients with Hypospermatogenesis
por: D’Aurora, Marco, et al.
Publicado: (2017)