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Article

[Kallmann syndrome: a historical [corrected] clinical and molecular review].

Arquivos brasileiros de endocrinologia e metabologia - 1 Feb 2008

Ribeiro Rogério Silicani, Abucham Julio

Abstract excerpt

Kallmann syndrome (KS), the association of hypogonadotropic hypogonadism and anosmia, was described by Maestre de San Juan in 1856 and characterized as a hereditary condition by Franz Josef Kallmann in 1944. Many aspects such as pathogeny, phenotype and genotype in KS were described in the last fifteen years. The knowledge of this condition has grown fast, making it difficult to update. Here we review historical...

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Source

Identifiers

PMID: 18345392
DOI: 10.1590/s0004-27302008000100004

Genes

FGFR1
PROK2
PROKR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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