The Focus Foundation’s publication on Novel Neurocognitive Profile in a Minority of Males with 47,XXY (Klinefelter Syndrome) has been published!
We are excited to announce that our article regarding the Neurocognitive Study of Boys with 47XXY, or Klinefelter Syndrome, was recently published by the Journal of Developmental & Behavioral Pediatrics! Our team is happy to share this study with the public and proud that it is co-authored by our very own Carole Samango-Sprouse and Teresa S. Sadeghin. The abstract for Novel Neurocognitive Profile in a Minority of Males with 47,XXY (Klinefelter syndrome) is currently available online. The article will be published in print in the upcoming issue of the official Journal of Developmental & Behavioral Pediatrics!
The Focus Foundation is proud to continue its goal to spread awareness and provide research, treatments, and facts about the 47,XXY Chromosomal Variation in males, also referred to as Klinefelter Syndrome.
Subscribe, buy, or request permission to use or download the full article about our Neurocognitive Study of Boys with 47XXY, or Klinefelter Syndrome, here: Novel Neurocognitive Profile in a Minority of Males with 47,XXY (Klinefelter syndrome)
The Focus Foundation is happy to share this new 47, XXY research with healthcare professionals, families, and parents of those with 47, XXY (Klinefelter syndrome). We hope to continue partnerships with other researchers to continue studies like these in the hopes of demystifying 47, XXY chromosomal variation, debunking misconceptions, and gaining helpful information to help with the treatment of chromosomal variations
Our Foundation specializes in X & Y Chromosomal Variation Disorders such as Klinefelters 47, Testosterone, Dyslexia, Dyspraxia, ADHD, and other Genetic Disorders. For more information please contact us or schedule a consultation at: thefocusfoundation.org/contact-us
