Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Clinical Management of Congenital Hypogonadotropic Hypogonadism

29 Jan 2019

Abstract excerpt

The initiation and maintenance of reproductive capacity in humans is dependent on pulsatile secretion of the hypothalamic hormone GnRH. Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder that results from the failure of the normal episodic GnRH secretion, leading to delayed puberty and infertility. CHH can be associated with an absent sense of smell, also termed Kallmann syndrome, or with other...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Share to Hypothalamic control of reproductive hormones
Share to Sexual Differentiation and Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 30698671
DOI: 10.1210/er.2018-00116

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical Management of Congenital Hypogonadotropic HypogonadismPMID 30698671Read ↗

European Consensus Statement on congenital hypogonadotropic hypogonadism—pathogenesis, diagnosis and treatmentSemantic proximity Read ↗

Congenital Hypogonadotropic Hypogonadism and Kallmann Syndrome: Past, Present, and FutureSemantic proximity Read ↗

Genetic Basis and Heterogeneity of Congenital Hypogonadotropic Hypogonadism.Semantic proximity Read ↗

Genetics of Idiopathic Hypogonadotropic HypogonadismSemantic proximity Read ↗

Non-syndromic congenital hypogonadotropic hypogonadism: clinical presentation and genotype-phenotype relationships.Semantic proximity Read ↗

Kallmann syndrome: Diagnostics and management.Semantic proximity Read ↗

A Review of Kallmann Syndrome: Genetics, Pathophysiology, and Clinical ManagementSemantic proximity Read ↗

Genetics of hypogonadotropic hypogonadism.Semantic proximity Read ↗

Congenital hypogonadotropic hypogonadism in females: clinical spectrum, evaluation and genetics.Semantic proximity Read ↗

Genetic and phenotypic differences between sexes in congenital hypogonadotropic hypogonadism (CHH): Large cohort analysis from a single tertiary centre.Semantic proximity Read ↗

Genetics defects in GNRH1: a paradigm of hypothalamic congenital gonadotropin deficiency.Semantic proximity Read ↗

Congenital idiopathic hypogonadotropic hypogonadism: evidence of defects in the hypothalamus, pituitary, and testes.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.