Welcome - Kallmann syndrome (KS) Community
What is Kallmann syndrome (KS) ?
Kallmann syndrome is a rare congenital hormonal condition characterised by failure to start or to fully complete puberty. It is a form of hypogonadotropic hypogonadism.
Source: HPOYHHKallmann syndrome (KS) Resources
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Partners and Patient Groups
RareConnect is a patient-led initiative. Patient organisations partner with EURORDIS, itself an international patient organisation, to create communities and provide moderators from within their network. The following patient groups are official partners of this community.