Kaur Ruveena, O'Sullivan Susannah
Department of Endocrinology, Greenlane Clinical Centre, Auckland 1051, New Zealand.
JCEM Case Rep. 2024 Jun 21;2(6):luae104. doi: 10.1210/jcemcr/luae104. eCollection 2024 Jun.
Turner syndrome (TS) is the most common sex chromosome disorder affecting females and is usually diagnosed within the first 3 decades of life. It can present with primary amenorrhea or infertility and often has a typical phenotype, with associated medical conditions that require lifelong surveillance. We report the case of a 76-year-old female with a history of osteoporosis and vertebral fractures who presented to our specialist osteoporosis clinic following a neck of femur fracture. She revealed a history of short stature and primary amenorrhea as a young woman, with limited investigation and treatment. Her other medical history included coeliac disease, hypertension, and hearing and vision abnormalities. Given her phenotype, the patient was referred for a karyotype at age 76, which was consistent with mosaic TS (45, X in 78% of cells and 46, X, r(Y) in the remaining cells). We review reports of other cases of marked delay in TS diagnosis and discuss the consequences of a late diagnosis.
特纳综合征(TS)是影响女性最常见的性染色体疾病,通常在生命的前三十年被诊断出来。它可表现为原发性闭经或不孕,且往往具有典型的表型,并伴有需要终身监测的相关疾病。我们报告了一例76岁女性患者,她有骨质疏松症和椎体骨折病史,因股骨颈骨折前来我们的骨质疏松专科门诊就诊。她透露年轻时有身材矮小和原发性闭经病史,当时检查和治疗有限。她的其他病史包括乳糜泻、高血压以及听力和视力异常。鉴于她的表型,该患者在76岁时被转诊进行核型分析,结果与嵌合型TS一致(78%的细胞为45,X,其余细胞为46,X,r(Y))。我们回顾了其他TS诊断明显延迟的病例报告,并讨论了延迟诊断的后果。