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Article

Reversal of congenital hypogonadotropic hypogonadism in a man with Kallmann syndrome due to SOX10 mutation.

Clinical endocrinology - 1 Dec 2016

Maione Luigi, Brailly-Tabard Sylvie, Nevoux Jérôme, Bouligand Jérôme, Young Jacques

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Share to Androgens
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Share to Luteinizing Hormone

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 27616149
DOI: 10.1111/cen.13231

Genes

SOX10

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Reversal of congenital hypogonadotropic hypogonadism in a man with Kallmann syndrome due to SOX10 mutation.PMID 27616149Read ↗

Hypogonadotropic hypogonadism in a female patient previously diagnosed as having waardenburg syndrome due to a sox10 mutation.Semantic proximity Read ↗

Diagnosis and genetic analysis of a case of Waardenburg syndrome type 2 with hypogonadotropic hypogonadism caused by SOX10 gene deletion.Semantic proximity Read ↗

Novel variants in the SOX11 gene: additional evidence for the involvement of SOX11 in hypogonadotropic hypogonadismSemantic proximity Read ↗

A de novo SOX11 mutation causing hypogonadotropic hypogonadism: a case report and literature review.Semantic proximity Read ↗

The genetics of hypogonadotropic hypogonadism.Semantic proximity Read ↗

SOX2 nonsense mutation in a patient clinically diagnosed with non-syndromic hypogonadotropic hypogonadism.Semantic proximity Read ↗

Savelyeva LV. Isolated hypogonadotropic hypogonadism caused by a mutation in the WDR11 gene: a clinical case reportSemantic proximity Read ↗

Reversible congenital hypogonadotropic hypogonadism in patients with CHD7, FGFR1 or GNRHR mutations.Semantic proximity Read ↗

A novel mutation in SOX2 causes hypogonadotropic hypogonadism with mild ocular malformation.Semantic proximity Read ↗

Hypogonadotropic hypogonadism in an adult female with a heterozygous hypomorphic mutation of SOX2Semantic proximity Read ↗

Kallmann syndrome: a case of hypogonadotropic hypogonadism.Semantic proximity Read ↗

Reversible Kallmann Syndrome, Delayed Puberty, and Isolated Anosmia Occurring in a Single Family with a Mutation in the Fibroblast Growth Factor Receptor 1 GeneSemantic proximity Read ↗

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