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Article

Kallmann syndrome in two sisters with other developmental anomalies also affecting their father.

Clinical genetics - 1 Jan 1993

Levy C M, Knudtzon J

Abstract excerpt

The classical features of Kallmann syndrome with anosmia and hypogonadotropic hypogonadism were observed in two sisters aged 13 and 19. They had additional malformations including anosmia, bilateral vesico-ureteral reflux and unilateral hearing loss. One of the girls had unilateral coloboma of the optic nerve. The father had unilateral hearing loss and duplication of the left ureter; he died of an unrecognized...

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Identifiers

PMID: 8462198
DOI: 10.1111/j.1399-0004.1993.tb04451.x

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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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