ReviewEndocrinology and metabolism clinics of North America2016
Diagnosis and Clinical Genetics of Cushing Syndrome in Pediatrics.
Review in Endocrinology and metabolism clinics of North America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03831958 (Long-Term Follow-UP of Survivors of Pediatric Cushing Disease), which is not on this map. Cited by 18 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Long-Term Follow-UP of Survivors of Pediatric Cushing Disease
Who cites it
18 citing papers in PubMed, 46 citations in OpenAlex.
- Growth Retardation in an Adolescent Secondary to Cushing's Disease Caused by a Pituitary Microadenoma: A Case Report.Reports (MDPI) · 2026Article
- Adrenal Cushing's syndrome in children.Frontiers in endocrinology · 2023Review
- Case Report: Severe McCune-Albright syndrome presenting with neonatal Cushing syndrome: navigating through clinical obstacles.Frontiers in endocrinology · 2023Article
- Treatment of Primary Pigmented Nodular Adrenocortical Disease.Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme · 2022Review
- Topical corticosteroid-induced iatrogenic cushing syndrome in an infant; a case report with literature review.Annals of medicine and surgery (2012) · 2021Article
- Cushing's syndrome in early infancy due to isolated sporadic bilateral micronodular adrenocortical disease associated with myosin heavy chain 8 mutation: diagnostic challenges, too many!BMJ case reports · 2020Article
- Identifying underlying medical causes of pediatric obesity: Results of a systematic diagnostic approach in a pediatric obesity center.PloS one · 2020Observational
- Cushing's Disease.Journal of clinical medicine · 2019Review
- Large Genomic Aberrations in Corticotropinomas Are Associated With Greater Aggressiveness.The Journal of clinical endocrinology and metabolism · 2019Article
- Clinical characteristics and surgical outcome in USP8-mutated human adrenocorticotropic hormone-secreting pituitary adenomas.Endocrine · 2019Article
- Infantile Iatrogenic Cushing Syndrome due to Topical Steroids.Case reports in pediatrics · 2019Article
- SELLA TURCICA 3T MAGNETIC RESONANCE IMAGING IN THE DIAGNOSIS OF CUSHING'S DISEASE IN CHILDREN: TWO CASE REPORTS.Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo · 2019Article
- Incidence of Autoimmune and Related Disorders After Resolution of Endogenous Cushing Syndrome in Children.Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme · 2018Article
- Neonatal Cushing Syndrome: A Rare but Potentially Devastating Disease.Clinics in perinatology · 2018Review
- Decreased lymphocytes and increased risk for infection are common in endogenous pediatric Cushing syndrome.Pediatric research · 2018Article
- Detection of new potentially pathogenic mutations in two patients with primary pigmented nodular adrenocortical disease (PPNAD) - case reports with literature review.Endokrynologia Polska · 2018Review
- Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease.The Journal of clinical endocrinology and metabolism · 2017Article
- Flushing in (neuro)endocrinology.Reviews in endocrine & metabolic disorders · 2016Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author at 1 institution in 1 country.
Funding
Abstract
Endogenous Cushing syndrome (CS) in pediatrics is rare; it may be caused by tumors that produce corticotropin in the pituitary gland or elsewhere, tumors that produce corticotropin-releasing hormone anywhere, and adrenocortical masses that produce cortisol. Adrenocortical cancer is a rare cause of CS in children but should be excluded first. CS in children is often caused by germline or somatic mutations with implications for patient prognosis and for their families. CS should be recognized early in children; otherwise, it can lead to significant morbidity and mortality. Patients with suspected CS should be referred to specialized clinical centers for workup.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.