在生命的第八个十年诊断出特纳综合征。

JCEM case reports Pub Date : 2024-06-21 eCollection Date: 2024-06-01 DOI:10.1210/jcemcr/luae104
Ruveena Kaur, Susannah O'Sullivan
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摘要

特纳综合征(Turner Syndrome,TS)是影响女性的最常见的性染色体疾病,通常在患者出生后 30 年内被诊断出来。它可表现为原发性闭经或不孕,通常具有典型的表型,并伴有需要终身监护的相关疾病。我们报告了一例 76 岁女性骨质疏松症患者的病例,她有骨质疏松症和椎体骨折病史,股骨颈骨折后到我们的骨质疏松症专科门诊就诊。她年轻时曾有身材矮小和原发性闭经的病史,但检查和治疗都很有限。她的其他病史包括乳糜泻、高血压、听力和视力异常。鉴于她的表型,患者在 76 岁时被转诊进行核型检查,结果与镶嵌型 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 诊断明显延迟病例的报告,并讨论了延迟诊断的后果。
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A Diagnosis of Turner Syndrome in the Eighth Decade of Life.

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.

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