Genotyping of a Chinese family with 46,XX and 46,XY 17-hydroxylase deficiency |
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| Authors: | Qinjie Tian Fengxia Yao Guihua Sha Shangzhi Huang Hung Tseng Adolf E Schindler |
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| Institution: | 1. Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, Chinaqinjietn@yahoo.com;3. Clinical Research Laboratory, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China;4. Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China;5. Department of Genetics, Basic Medical Institute, Peking Union Medical College, Chinese Academy of Medical Science, Beijing, China;6. Department of Dermatology, School of Medicine, University of Pennsylvania, Philadelphia, USA;7. Institute for Medical Research and Education, Essen, Germany |
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| Abstract: | Background.?17-Hydroxylase deficiency is a rare form of congenital adrenal hyperplasia caused by CYP17A1 gene mutations.Method.?A 46,XY and a 46,XX Chinese patients with 17-hydroxylase deficiency in a family and their four generations family members were genotyped by PCR-sequencing method.Results.?Two CYP17 gene mutations were identified from these patients. Among them, IVS1-1G > A was a novel splicing mutation which disrupted the acceptor signal of exon 2 and might create a new exon after exon 1. The indel mutation of TAC329AA was a one-base deletion mutation and one-base change at codon 329 in exon 6.Conclusion.?The results confirmed the diagnosis of 17-hydroxylase deficiency in these two patients and their autosome recessive heritage mode. The TAC329AA indel mutation had been identified in several reports of Chinese and Asian, suggesting that codon 329 was an unstable point of the CYP17 gene and this mutation was a prevalent CYP17 mutation in the Asian population. Although the noval mutation IVS1-1G > A founded in this family need more study to know its machinism of interrupting P450c17 function. |
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| Keywords: | 17-hydroxylase deficiency (17OHD) CYP17A1 gene family genotyping gene mutations |
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