Clinical characteristics and molecular diagnosis in 2 cases of P450 oxidoreductase deficiency
10.3760/cma.j.issn.1000-6699.2018.11.006
- VernacularTitle:两例细胞色素P450氧化还原酶缺陷症的临床特点和分子诊断
- Author:
Wencui WANG
1
;
Lei YE
;
Zuwei YANG
;
Huiying JIA
;
Jie ZHANG
;
Yu ZHAO
;
Weiqing WANG
;
Guang NING
;
Shouyue SUN
Author Information
1. 上海交通大学医学院附属瑞金医院内分泌科
- Keywords:
P450 oxidoreductase deficiency;
Congenital adrenal hyperplasia;
POR gene
- From:
Chinese Journal of Endocrinology and Metabolism
2018;34(11):926-930
- CountryChina
- Language:Chinese
-
Abstract:
Objective To analyze clinical characteristics and gene mutation of two patients diagnosed with P450 oxidoreductase deficiency(PORD). Methods Clinical data of 2 patients with PORD was collected from Ruijin hospital. POR gene mutation was analyzed by PCR-Sanger sequencing. A retrospective analysis of literatures concerning PORD was performed. Results Patient 1, female, 16 years old, with 46,XX karyotype, presented with anorectal anomalies, clitoral hypertrophy at birth and irregular menstruation; Patient 2, female, 32 years old, with 46,XX karyotype, showed irregular menstruation and infertility, both without obvious skeletal deformity. Genetic test of POR gene mutation revealed that patient 1 carried a homozygous missense mutation (R457H) and patient 2 carried a heterozygous mutation (R223X/ Y607C). The two mutations (R223X and Y607C) are reported for the first time in China. Conclusion P450 oxidoreductase deficiency which caused by mutations in POR gene has a variety of clinical manifestations, including abnormal steroid hormone synthesis with or without Antley-Bixler syndrome. The affirmative diagnosis should rely on steroid hormone measurement and POR gene analysis.
