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Case Reports
. 2016 Oct;64(10):106-107.

Kallman Syndrome

Affiliations
  • PMID: 27766822
Case Reports

Kallman Syndrome

N Nand et al. J Assoc Physicians India. 2016 Oct.

Abstract

Kallman syndrome (KS) is a rare genetic disorder characterized clinically by failure to attain puberty or failure to fully complete it along with an absent or impaired sense of smell with absence of bilateral olfactory bulbi and sulci alongwith absent olfactory tracts. Only very few cases of Kallman syndrome have been reported in females in Indian population.

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