Jo, H.C., Lee, S.W., Jung, H.J. and Park, J.E. (2016) Esthesioneuroblastoma in a Boy with 47, XYY Karyotype. Korean Journal of Pediatrics, 59, S92-S95.
https://doi.org/10.3345/kjp.2016.59.11.S92

has been cited by the following article:

• TITLE: Jacob’s Syndrome and Deficiency of 11-Beta-Hydroxylase Enzyme Association Revealed by a Statural Advance: A Case Report

  AUTHORS: Wafa Aitifali, Fatima Zahra Lahmamssi, Sana Abourazzak, Laila Bouguenouch, Moustapha Hida

  KEYWORDS: Jacob’s Syndrome, 47XYY Syndrome, 11-Beta-Hydroxylase Deficiency

  JOURNAL NAME: Case Reports in Clinical Medicine, Vol.12 No.6, June 30, 2023

  ABSTRACT: 47XYY syndrome is a rare sex chromosome variant with an extra Y chromosome. Most patients with a 47XYY karyotype have a normal phenotype. This disorder seems to be associated with a higher risk of developing behavior and cognitive problems, tall stature and infertility in adulthood. We report here a rare case of 47, XYY syndrome associated with an 11-beta-hydroxylase deficiency revealed by a stature advance along with precocious puberty after obtaining informed consent from parents. To our knowledge, this is the first case reported in the literature.