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 girl with Cushing's syndrome due to primary pigmented nodular adrenocortical disease].

Nederlands tijdschrift voor geneeskunde - 28 Oct 2006

Bocca G, van Mil E G A H, Voorhoeve P G, Wijnaendts L C D, Delemarre-van de Waal H A

Abstract excerpt

A 12.5-year-old girl with diabetes mellitus type 1 presented with stunted growth and an increase in body weight. Also, her blood-sugar levels were difficult to manage. An adrenocorticotropin-(ACTH)-independent form of Cushing's syndrome was diagnosed. During the dexamethasone-suppression test, a paradoxical increase in urinary-free cortisol excretion was observed, which is a clear indication of primary pigmented...

Read the complete abstract on PubMed

Topics

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

Share to Adrenalectomy
Share to Adrenocorticotropic Hormone

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cushing Syndrome

Share to Cyclic AMP-Dependent Protein Kinases

Share to Dexamethasone

Share to Diabetes Mellitus, Type 1

Share to Hydrocortisone

Source

Identifiers

PMID: 17100132

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 girl with Cushing's syndrome due to primary pigmented nodular adrenocortical disease].PMID 17100132Read ↗

[A pedigree study of a patient with primary pigmented nodular adrenocortical disease and familial gene mutation].Semantic proximity Read ↗

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

Primary pigmented nodular adrenocortical disease and Cushing's syndrome.Semantic proximity Read ↗

[Clinical features and pathogenesis of Carney complex, a rare form of multiple endocrine neoplasia syndromes].Semantic proximity Read ↗

[Primary pigmented nodular adrenocortical disease (PPNAD)].Semantic proximity Read ↗

A rare case of familial Cushing's syndrome with a common presentation of weight gain due to a mutation of the PRKAR1A gene causing isolated primary pigmented nodular adrenocortical disease.Semantic proximity Read ↗

Primary pigmented nodular adrenocortical disease (PPNAD): single centre experienceSemantic proximity Read ↗

Cushing syndrome in a young woman due to primary pigmented nodular adrenal disease.Semantic proximity Read ↗

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

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

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

Update on primary micronodular bilateral adrenocortical diseasesSemantic proximity Read ↗

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