Da-Yong Cai
Abstract
Kallmann syndrome is a rare inherited disease,characterized by hypogonadism and accompanied by anosmia or hyposmia.To date,3 modes of inheritance and 5 genes related to Kallmann syndrome have been identified.This review focuses on the advances in the diagnosis,treatment and genetic studies of Kallmann syndrome.
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Kallmann syndrome is a rare inherited disease,characterized by hypogonadism and accompanied by anosmia or hyposmia.To date,3 modes of inheritance and 5 genes related to Kallmann syndrome have been identified.This review focuses on the advances in the diagnosis,treatment and genetic studies of Kallmann syndrome.
Key concepts: Kallmann syndrome, Hyposmia, Anosmia, Hypogonadotropic hypogonadism, Medicine, Disease, Inheritance (genetic algorithm), Endocrinology