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Dumeige, L., Chatelais, L., Bouvattier, C., De Kerdanet, M., Hyon, C., Esteva, B., et al. (2018) Should 45,X/46,XY Boys with No or Mild Anomaly of External Genitalia Be Investigated and Followed Up? European Journal of Endocrinology, 179, 181-190.
https://doi.org/10.1530/eje-18-0309

has been cited by the following article:

• TITLE: A Boy 45X/46XY Mosaicism with ADHD: A Case Report

  AUTHORS: Hsin-I Wu, Chang-Hsien Yu

  KEYWORDS: 45X/46XY Mosaicism, ADHD, Developmental Delay

  JOURNAL NAME: Case Reports in Clinical Medicine, Vol.13 No.12, December 17, 2024

  ABSTRACT: 45X/46XY mosaicism is a rare chromosome disease. The apparent prevalence of males and females with 45X/46XY is 5.6 and 2.1 per 100,000 liveborn males and females. We present a boy who had a developmental delay with hypospadias. He was referred to pediatric genetics and was diagnosed with 45X/46XY mosaicism by peripheral blood chromosome examination. During serial rehabilitation programs, his speech delay was caught up. But his poor attention and hyperactivity are obvious progressively. We should pay attention to these patients, not only physical conditions but also psychological problems.