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Article

Childhood growth of females with Kallmann syndrome and FGFR1 mutations.

Clinical endocrinology - 1 Jan 2015

Hero Matti, Laitinen Eeva-Maria, Varimo Tero, Vaaralahti Kirsi, Tommiska Johanna, Raivio Taneli

Abstract excerpt

OBJECTIVE: In search of phenotypic cues that would allow early detection of Kallmann syndrome (KS), we evaluated the paediatric phenotypes in a series of females with KS. DESIGN, PATIENTS AND MEASUREMENTS: In this retrospective cohort study, we investigated childhood growth in six females with KS due to mutations in FGFR1 and evaluated their reproductive phenotypes later in life. RESULTS: While growth during...

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Source

Identifiers

PMID: 24841555
DOI: 10.1111/cen.12504

Genes

FGFR1
SDS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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