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Jacob’s Syndrome and Deficiency of 11-Beta-Hydroxylase Enzyme Association Revealed by a Statural Advance: A Case Report
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作者 Wafa Aitifali Fatima Zahra Lahmamssi +2 位作者 Sana Abourazzak Laila Bouguenouch Moustapha Hida 《Case Reports in Clinical Medicine》 2023年第6期207-211,共5页
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 ... 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. 展开更多
关键词 Jacob’s syndrome 47xyy syndrome 11-Beta-Hydroxylase Deficiency
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