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Article

Two cases of Kallmann syndrome associated with empty sella.

Pituitary - 1 Jan 2008

Dallago Cristina Micheletto, Abech Denise Dotta, Pereira-Lima Julia Fernanda Semmelmann, Leães Caroline Garcia Soares, Batista Rafael Loch, Trarbach Ericka Barbosa, Oliveira Miriam da Costa

Abstract excerpt

Kallmann syndrome (KS) is a developmental disease characterized by the association of isolated hypogonadotropic hypogonadism and anosmia/hyposmia. We report an unusual presentation of two females with KS and empty sella. These females, aged at 20 and 29-year-old, presented primary amenorrhea with...

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Source

Identifiers

PMID: 17530415
DOI: 10.1007/s11102-007-0043-9

Genes

FGFR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17530415-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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