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Kallmann syndrome

Modality: MRI (T2)

From the case:

Kallmann syndrome - “Kallmann syndrome is rare, but has characteristic imaging findings which should be sought in patients with delayed onset of puberty / hypogonadism. ”

Used in the following article:

  • Kallmann syndrome - “Kallmann syndrome (KS) is a rare genetic disorder characterised by hypogonadotropic hypogonadism associated with anosmia or hyposmia. When anosmia ...”

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