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

Obesity in Prader-Willi syndrome: physiopathological mechanisms, nutritional and pharmacological approaches.

Journal of endocrinological investigation - 1 Oct 2021

Muscogiuri G, Barrea L, Faggiano F, Maiorino M I, Parrillo M, Pugliese G, Ruggeri R M, Scarano E, Savastano S, Colao A

Abstract excerpt

Prader-Willi syndrome (PWS) is a genetic disorder caused by the lack of expression of genes on the paternally inherited chromosome 15q11.2-q13 region. The three main genetic subtypes are represented by paternal 15q11-q13 deletion, maternal uniparental disomy 15, and imprinting defect. Clinical picture of PWS changes across life stages. The main clinical characteristics are represented by short stature,...

Read the complete abstract on PubMed

Topics

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

Share to Genetic Syndromes and Imprinting
Share to Genetics and Neurodevelopmental Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Obesity

Share to Pancreatic function and diabetes

Share to Phenotype

Share to Prader-Willi Syndrome

Source

Open in PubMed Open full text

Identifiers

PMID: 33891302
DOI: 10.1007/s40618-021-01574-9
PMCID: PMC8421305

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Obesity in Prader-Willi syndrome: physiopathological mechanisms, nutritional and pharmacological approaches.PMID 33891302Read ↗

Prader-Willi Syndrome: Clinical AspectsSemantic proximity Read ↗

[Prader-Willi syndrome].Semantic proximity Read ↗

[Prader-Willi syndrome in 2015].Semantic proximity Read ↗

Prader-Willi Syndrome: Clinical Genetics and Diagnostic Aspects with Treatment Approaches.Semantic proximity Read ↗

Clinical, molecular genetics and therapeutic aspects of syndromic obesity.Semantic proximity Read ↗

Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation.Semantic proximity Read ↗

Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.Semantic proximity Read ↗

Disentangling ingestive behavior-related phenotypes in Prader-Willi syndrome: Integrating information from nonclinical studies and clinical trials to better understand the pathophysiology of hyperphagia and obesity.Semantic proximity Read ↗

Advances in genetic mechanisms of hypothalamic dysfunction in Prader-Willi syndrome.Semantic proximity Read ↗

Prader Willi syndrome: advances in genetics.Semantic proximity Read ↗

Obesity in Childhood and Adolescence, Genetic Factors.Semantic proximity Read ↗

Prader-Willi Syndrome - Clinical Genetics, Diagnosis and Treatment Approaches: An UpdateSemantic proximity Read ↗

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