A case of 49,XXXYY followed-up from infancy to adulthood with review of literature
49,XXXYY is an extremely rare sex chromosomal aneuploidy (SCA), with only seven cases reported worldwide to date. Among these cases, only three have been documented into adulthood. Moreover, no cases of 49,XXXYY have been reported in Japan. This SCA has been identified in two scenarios: in vitro fer...
Saved in:
Main Authors: | Junko Kanno, Akinobu Miura, Sayaka Kawashima, Hirohito Shima, Dai Suzuki, Miki Kamimura, Ikuma Fujiwara, Masayuki Kamimura, Mitsugu Uematsu, Masataka Kudo, Atsuo Kikuchi |
---|---|
Format: | Article |
Language: | English |
Published: |
The Japan Endocrine Society
2024-07-01
|
Series: | Endocrine Journal |
Subjects: | |
Online Access: | https://www.jstage.jst.go.jp/article/endocrj/71/7/71_EJ24-0015/_html/-char/en |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
The immunogenicity of PRV ΔgE/TK/UL49.5 three-gene-deleted vaccine in mice
by: Chenmeng Ding, et al.
Published: (2025-02-01) -
Psychiatric-Mental Health Nursing : the thrapeutic use of self /
by: Birckhead, Loretta M.
Published: (1989) -
A discussion of anesthesiologically relevant aspects of Klinefelter syndrome -a case report-
by: Christine Gaik, et al.
Published: (2025-02-01) -
Diabetic Ketoacidosis in Klinefelter Syndrome Sans Malignancy with Unusually Elevated Levels of CEA: A Case Report
by: Wo X, et al.
Published: (2025-01-01) -
Perinatal Outcome of Fetal Echogenic Bowel: A Single-Center Retrospective Cohort Study
by: Hidayet Sal, et al.
Published: (2021-04-01)