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Volume 19, Issue 3 (May 2017) 19, 386–387; DOI:10.4103/1008-682X.170865
Genetic sequencing of a patient with Kallmann syndrome plus 5α-reductase type 2 deficiency
Wen Ji, Lu-Yao Zhang, Fu-Cheng Li, Yu Wang, Wei He, Qi-Qi Yin, Zhi-Hong Liao
1Department of Endocrinology, 1st Affiliated Hospital of Sun Yat‑sen University,
Guangzhou, 510080, China; 2Department of Medical Genetics, Genome Research
Center, Zhongshan School of Medicine, Sun Yat‑sen University, Guangzhou,
510080, China.
Correspondence: Prof. ZH Liao (liaozhh@mail.sysu.edu.cn)
Date of Submission 07-Jun-2015 Date of Decision 26-Jul-2015 Date of Acceptance 29-Oct-2015 Date of Web Publication 15-Jan-2016
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Dear Editor,
Kallmann syndrome (KS) is a phenotypically and genetically heterogeneous disorder featured by hypogonadotropic hypogonadism and congenital hyposmia or anosmia, accompanined with renal dysplasia, hearing loss, and craniofacial defects sometimes. More than 20 genes have been identified causing KS either alone or in combination.
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