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

PRKAR1A mutations in primary pigmented nodular adrenocortical disease.

Pituitary - 1 Jan 2006

Cazabat Laure, Ragazzon Bruno, Groussin Lionel, Bertherat Jérôme

Abstract excerpt

Primary Pigmented Nodular Adrenocortical Disease (PPNAD) is a rare primary bilateral adrenal defect causing corticotropin-independent Cushing's syndrome. It occurs mainly in children and young adults. Macroscopic appearance of the adrenals is characteristic with small pigmented micronodules obser...

Read the complete abstract on PubMed

Topics

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

Share to Cushing Syndrome
Share to Cyclic AMP
Share to Cyclic AMP-Dependent Protein Kinase RIalpha Subunit

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cyclic AMP-Dependent Protein Kinases

Share to Gene Expression Regulation, Enzymologic

Share to Hormones

Share to Multiple Endocrine Neoplasia

Share to Pigmentation Disorders

Source

Identifiers

PMID: 17036196
DOI: 10.1007/s11102-006-0266-1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17036196-2026-09-02.1. Manifest publication-graph-cohort-2026-09-02.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

PRKAR1A mutations in primary pigmented nodular adrenocortical disease.PMID 17036196Read ↗

Mutations of the PRKAR1A gene in Cushing's syndrome due to sporadic primary pigmented nodular adrenocortical disease.Semantic proximity Read ↗

A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds.Semantic proximity Read ↗

Adrenal Pathophysiology: Lessons from the Carney ComplexSemantic proximity Read ↗

A novel PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease and the Carney complex.Semantic proximity Read ↗

A Novel Mutation in the type Iα Regulatory Subunit of Protein Kinase A (PRKAR1A) in a Cushing's Syndrome Patient with Primary Pigmented Nodular Adrenocortical Disease.Semantic proximity Read ↗

PRKAR1A mutation causing pituitary-dependent Cushing disease in a patient with Carney complex.Semantic proximity Read ↗

Children with Cushing's syndrome: Primary Pigmented Nodular Adrenocortical Disease should always be suspected.Semantic proximity Read ↗

Genetics of micronodular adrenal hyperplasia and Carney complex.Semantic proximity Read ↗

Carney complex with adrenocorticotropic hormone-independent Cushing syndrome with PRKAR1A gene variant: a case report.Semantic proximity Read ↗

Association of the M1V PRKAR1A mutation with primary pigmented nodular adrenocortical disease in two large families.Semantic proximity Read ↗

Familial isolated primary pigmented nodular adrenocortical disease associated with a novel low penetrance PRKAR1A gene splice site mutation.Semantic proximity Read ↗

The clinical characteristics and pathogenic variants of primary pigmented nodular adrenocortical disease in 210 patients: a systematic review.Semantic proximity Read ↗

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