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

[Primary adrenal insufficiency in children].

Nederlands tijdschrift voor geneeskunde - 21 May 2005

Rijlaarsdam R S, van Diepen M M L, Wit J M

Abstract excerpt

Three boys, aged 5, 11 and 14 years, were admitted due to vomiting, fatigue and dehydration, and a 10-year-old boy was admitted due to circulatory and respiratory insufficiency. Two had Addison's disease, one had a late presentation of congenital adrenal hypoplasia due to a DAX-1 mutation and in one adrenal insufficiency was the first manifestation ofadrenoleukodystrophia. The boys recovered after treatment. It...

Read the complete abstract on PubMed

Topics

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

Share to Addison Disease
Share to Adrenal Insufficiency
Share to Adrenoleukodystrophy

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, X

Share to DAX-1 Orphan Nuclear Receptor

Share to Receptors, Retinoic Acid

Share to Repressor Proteins

Share to Treatment Outcome

Source

Identifiers

PMID: 15940915

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Primary adrenal insufficiency in children].PMID 15940915Read ↗

[Acute adrenal insufficiency in the newborn].Semantic proximity Read ↗

Primary Adrenal Insufficiency in Childhood: Data From a Large Nationwide Cohort.Semantic proximity Read ↗

[Adrenal insufficiency as the only manifestation of X-linked adrenoleukodystrophy].Semantic proximity Read ↗

[Clinical features of 9 patients with X-linked adrenal hypoplasia congenita caused by DAX1/NR0B1 gene mutations].Semantic proximity Read ↗

[Abnormalities in the development of adrenal gland].Semantic proximity Read ↗

[X-linked congenital adrenal hypoplasia].Semantic proximity Read ↗

X-linked Congenital Adrenal Hypoplasia with a Novel NR0B1/DAX Gene Mutation.Semantic proximity Read ↗

Adrenal insufficiency updates in children.Semantic proximity Read ↗

Extreme hyponatremia in an infant with congenital adrenal hypoplasia due to a novel NR0B1 (DAX-1) mutation.Semantic proximity Read ↗

Congenital Adrenal Hypoplasia: Clinical Spectrum, Experience with Hormonal Diagnosis, and Report on New Point Mutations of the DAX-1 GeneSemantic proximity Read ↗

[Mutation in DAX-1 gene as a cause of primary hypoadrenalism and hypogonadotropic hypogonadism].Semantic proximity Read ↗

[Adrenal medullary hyperplasia].Semantic proximity Read ↗

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