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46,XX 患者中诊断出的细胞色素 P450 氧化还原酶缺乏症的临床特征和分子病因学

Clinical Characteristics and Molecular Aetiology of Cytochrome P450 Oxidoreductase Deficiency Diagnosed in 46,XX Patients.

作者信息

Zhang Duoduo, Ding Lelei, Deng Shan, Tian Qinjie

机构信息

Department of Obstetrics and Gynecology, National Clinical Research Center for Obstetric & Gynecologic Diseases, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, 100730, People's Republic of China.

Center for Rare Diseases Research, Chinese Academy of Medical Sciences, Beijing, 100730, People's Republic of China.

出版信息

Reprod Sci. 2025 Jul;32(7):2474-2483. doi: 10.1007/s43032-025-01878-8. Epub 2025 Jun 18.

Abstract

P450 oxidoreductase deficiency (PORD) affects cytochrome enzyme activities, causing various symptoms, such as adrenal insufficiency, disorders of sex development and skeletal malformations. This study aims to elucidate the clinical manifestations, genotype characteristics, diagnosis and management of 46,XX karyotype patients with PORD in China. A retrospective study included twelve 46,XX PORD patients in a Chinese tertiary medical center from 2004 to 2024. The patients' clinical characteristics were summarized based on manifestations, hormone profiles, and responses to treatments. The age of first visit was 7-31 years. Except for one young girl presenting with ambiguous genitalia since born, 11 patients presented with either abnormal menses or multiple ovarian cysts. Six patients showed masculinization of their external genitalia, and ten patients showed varying degrees of skeletal deformity. Progesterone was elevated and ovarian reserve was poor in all patients. The most frequent POR variant, c.1370G > A, located in exon 11 occurred in 11/12 patients with an allele frequency of 87.5% (21/24). Two novel nonsense mutations, c.1684dupG and c.2040dupC, were identified and assessed as pathogenic and likely pathogenic by ACMG, respectively. The c.1370G > A might be a dominant mutation type of POR in China. Female patients with PORD have a vulnerable ovarian reserve, and their ovarian macrocysts can be managed conservatively for fertility preservation. This study specifically focuses on PORD in 46,XX Chinese individuals, which implies its genetic causes with novel genetic findings and summarizes the puzzling spectrum of clinical manifestations.

摘要

细胞色素P450氧化还原酶缺乏症(PORD)会影响细胞色素酶的活性,导致多种症状,如肾上腺功能不全、性发育障碍和骨骼畸形。本研究旨在阐明中国46,XX核型PORD患者的临床表现、基因型特征、诊断和治疗。一项回顾性研究纳入了2004年至2024年在中国一家三级医疗中心就诊的12例46,XX PORD患者。根据临床表现、激素水平和治疗反应总结患者的临床特征。首次就诊年龄为7至31岁。除一名自出生就出现生殖器模糊的年轻女孩外,11例患者出现月经异常或多个卵巢囊肿。6例患者出现外生殖器男性化,10例患者出现不同程度的骨骼畸形。所有患者孕酮升高且卵巢储备功能差。最常见的POR变异体c.1370G > A位于第11外显子,在12例患者中的11例出现,等位基因频率为87.5%(21/24)。鉴定出两个新的无义突变c.1684dupG和c.2040dupC,美国医学遗传学与基因组学学会(ACMG)分别将其评估为致病和可能致病。c.1370G > A可能是中国POR的主要突变类型。PORD女性患者的卵巢储备功能脆弱,其卵巢大囊肿可采取保守治疗以保留生育能力。本研究专门聚焦于中国46,XX个体的PORD,揭示了其遗传原因及新的遗传发现,并总结了令人困惑的临床表现谱。

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