Kallman Syndrome
- PMID: 27766822
Kallman Syndrome
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.
© Journal of the Association of Physicians of India 2011.
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