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Article

Renal dysgenesis and KAL1 gene defects in patients with sporadic Kallmann syndrome.

Fertility and sterility - 1 Nov 2007

Georgopoulos Neoklis A, Koika Vasiliki, Galli-Tsinopoulou Assimina, Spiliotis Bessie E, Adonakis George, Keramida Maria K, Sgourou Argyro, Koufogiannis Kleanthis D, Papachatzopoulou Adamantia, Papavassiliou Athanasios G, Kourounis George, Vagenakis George A

Abstract excerpt

OBJECTIVE: To correlate the presence of renal agenesis/dysgenesis to the prevalence of KAL1 gene defects in patients with sporadic Kallmann syndrome (KS). DESIGN: Prospective assessment of renal structure and DNA sequence analysis of the KAL1 gene. SETTING: Outpatient clinics of the divisions of endocrinology of university hospitals. PATIENT(S): Sixteen male patients with sporadic KS. INTERVENTION(S): Assessment...

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Identifiers

PMID: 17603054
DOI: 10.1016/j.fertnstert.2006.12.044

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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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