Clinical characterization of epilepsy in children with chromosomal aberration 47, XXY
Abstract Objective The phenotype of the chromosomal aberration 47, XXY exhibits considerable heterogenicity. In addition, epilepsy is extremely uncommon in individuals with this chromosomal disorder. As a result, the clinical characteristics of epilepsy in these patients remain poorly understood. Me...
Main Authors: | Congjie Chen, Yuanyuan Luo, Xueqing Hou, Tingsong Li |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2023-08-01
|
Series: | Brain and Behavior |
Subjects: | |
Online Access: | https://doi.org/10.1002/brb3.3178 |
Similar Items
-
Update On The Clinical Perspectives And Care Of The Child With 47,XXY (Klinefelter Syndrome)
by: Samango-Sprouse CA, et al.
Published: (2019-10-01) -
Outcome of Intracytoplasmic Injection of Sperm Obtained by Testicular Sperm Extraction from 14 Azoospermic Men Suffering from 47,XXY Non-mosaic Klinefelter's Syndrome
by: Chun-Ming Chiang, et al.
Published: (2004-06-01) -
An Adolescent Boy with Klinefelter Syndrome and 47,XXY/46,XX Mosaicism: Case Report and Review of Literature
by: Tinka Hovnik, et al.
Published: (2022-04-01) -
Klinefelter syndrome in primary care: A case and review
by: Chad Richmond, et al.
Published: (2023-01-01) -
A rare case of lateral ovotesticular disorder with Klinefelter syndrome mosaicism 46, XX/47, XXY: An unusual presentation
by: Shyam M Talreja, et al.
Published: (2015-01-01)