Discover Community Create You

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

[A case of Kennedy-Alter-Sung (KAS) syndrome presenting as hypersexuality and elevated serum CK: usefulness of genetic analysis].

Rinsho shinkeigaku = Clinical neurology - 1 Mar 1996

Hokezu Y, Yanai S, Nagai M, Nagamatsu K, Yamamoto Y

Abstract excerpt

We report a unique case of KAS syndrome presenting as hypersexuality and elevated serum creatine kinase (CK). None of the other members of the patient's family had KAS. The patient had engaged in sexual behavior 4 approximately 5 times a week since his marriage. He did not have gynecomastia or hepatomegaly. Neurological examination revealed facial twitching and tongue atrophy and fasciculations. Mild to moderate...

Read the complete abstract on PubMed

Topics

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

Share to Creatine Kinase
Share to GPT gene
Share to Muscular Atrophy, Spinal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Pedigree

Share to Receptors, Androgen

Share to Syndrome

Source

Identifiers

PMID: 8741352

Genes

GPT

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[A case of Kennedy-Alter-Sung (KAS) syndrome presenting as hypersexuality and elevated serum CK: usefulness of genetic analysis].PMID 8741352Read ↗

[Study on clinical manifestation, genotype and genetic characteristics of two Kennedy disease pedigrees].Semantic proximity Read ↗

Type IV hyperlipoproteinemia and moderate instability of CAG triplet expansion in the androgen-receptor gene. Lipid, sex hormone and molecular study in a Chinese family with Kennedy-Alter-Sung disease.Semantic proximity Read ↗

Genotype and clinical phenotype analysis of a Family with Kennedy disease.Semantic proximity Read ↗

Endocrine and metabolic evaluation of classic Klinefelter syndrome and high-grade aneuploidies of sexual chromosomes with male phenotype: are they different clinical conditions?Semantic proximity Read ↗

Hypothyroidism secondary to hypothalamic-pituitary dysfunction may be part of the phenotype in klinefelter syndrome: a case-control study.Semantic proximity Read ↗

[Virilizing syndrome as a form of presentation of adrenal carcinoma in an toddler].Semantic proximity Read ↗

"Case Report: Klinefelter Syndrome Presenting With Dystonic Tremor: Expanding the Phenotypic Spectrum and Therapeutic Option".Semantic proximity Read ↗

A comprehensive endocrine description of Kennedy's disease revealing androgen insensitivity linked to CAG repeat length.Semantic proximity Read ↗

[Rare combination of dystrophinopathy and Klinefelter's syndrome in one patient].Semantic proximity Read ↗

Phenotypic differences in a large family with Kennedy's disease from the Middle Black Sea region of Turkey.Semantic proximity Read ↗

Ovarioleukodystrophy in Chinese Han: A case report.Semantic proximity Read ↗

[Morris syndrome: description of a case characterized by partial androgen insensitivity].Semantic proximity Read ↗

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