Cargando…

Pediatric Cushing Disease: Disparities in Disease Severity and Outcomes in the Hispanic and African American Populations

BACKGROUND: Little is known about the contribution of racial and socioeconomic disparities to severity and outcomes for children with Cushing disease (CD). METHODS: 129 children with CD, 45 Hispanic/Latino or African American (HI/AA) and 84 non-Hispanic White (non-HW), are included. A 10-point index...

Descripción completa

Detalles Bibliográficos
Autores principales:	Gkourogianni, Alexandra, Sinaii, Ninet, Jackson, Sharon H., Karageorgiadis, Alexander S., Lyssikatos, Charalampos, Belyavskaya, Elena, Keil, Margaret F., Zilbermint, Mihail, Chittiboina, Prashant, Stratakis, Constantine A., Lodish, Maya B.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	2017
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552413/ https://www.ncbi.nlm.nih.gov/pubmed/28422946 http://dx.doi.org/10.1038/pr.2017.58

Ejemplares similares

Aortic pulse wave velocity in children with Cushing syndrome: A window into a marker of early cardiovascular disease
por: Blain, Hailey, et al.
Publicado: (2019)

Decreased Lymphocytes and Increased Risk for Infection are Common in Endogenous Pediatric Cushing Syndrome
por: Tatsi, Christina, et al.
Publicado: (2017)

Lipoprotein particles in patients with pediatric Cushing disease and possible cardiovascular risks
por: Makri, Angeliki, et al.
Publicado: (2019)

MON-433 The Spectrum Of Growth Hormone Excess In Carney Complex: Characterizing A Common Finding In A Rare Syndrome
por: Tatsi, Christina, et al.
Publicado: (2019)

Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene
por: Nobel, Yael R, et al.
Publicado: (2016)

Patterns of thyroid hormone levels in pediatric medullary thyroid carcinoma patients on vandetanib therapy
por: Lodish, Maya, et al.
Publicado: (2015)

MON-190 Telomere Length as a Novel Prognostic Marker of Cushing Complications
por: Tatsi, Christina, et al.
Publicado: (2020)

OR24-6 Non-syndromic Cushing's Disease Due To CDKN1B Mutations: Novel Mutations And Phenotypic Features In A Large Pediatric Cohort
por: Hernández-Ramírez, Laura, et al.
Publicado: (2019)

SUN-356 The Effects of Selective Serotonin Reuptake Inhibitors on Urinary Free Cortisol in Patients with Carney Complex and Primary Pigmented Nodular Adrenocortical Disease
por: Kamilaris, Crystal, et al.
Publicado: (2019)

OR23-01 Intrapatient ACTH Variability in Cushing’s Disease: Prognostic Significance
por: Alvarez, Reinier, et al.
Publicado: (2020)

SAT-304 Pituitary Stem Cells May Drive Adenomas Causing Cushing’s Disease
por: Asuzu, David, et al.
Publicado: (2020)

SUN-058 Concurrent Hypercortisolism in Primary Aldosteronism Patients at a Tertiary Care Center: 2007-2017
por: Suzuki, Mari, et al.
Publicado: (2019)

Selective Serotonin Reuptake Inhibitors Increase Urinary Free Cortisol in Patients with Carney Complex and Primary Pigmented Nodular Adrenocortical Disease
por: Chrysavgi Kamilaris, Crystal Dawn, et al.
Publicado: (2021)

OR06-01 The Role of Germline Defects in Cushing’s Disease
por: Hernández-Ramírez, Laura C, et al.
Publicado: (2020)

Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease
por: Faucz, Fabio R., et al.
Publicado: (2017)

Genetics of Hypertension in African Americans and Others of African Descent
por: Zilbermint, Mihail, et al.
Publicado: (2019)

SAT-300 Evading Death: Noxa in Cushing’s Disease Pituitary Adenomas
por: Alvarez, Reinier, et al.
Publicado: (2020)

Bone Mineral Density in Patients with Inherited Bone Marrow Failure Syndromes
por: Shankar, Roopa Kanakatti, et al.
Publicado: (2017)

Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?
por: Martínez de LaPiscina, Idoia, et al.
Publicado: (2020)

Somatic PRKAR1A Gene Mutation in a Nonsyndromic Metastatic Large Cell Calcifying Sertoli Cell Tumor
por: Tatsi, Christina, et al.
Publicado: (2019)

RF01 | PMON167 Isolated Cushing's Disease Associated With Rare Germline SDHx Variants
por: Chittiboina, Prashant, et al.
Publicado: (2022)

Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing’s disease
por: Hernández-Ramírez, Laura C, et al.
Publicado: (2017)

Health-Related Quality of Life in Cushing Disease: Discrepancy Between Parent and Child Reports
por: Keil, Margaret F, et al.
Publicado: (2021)

THU214 Exploratory Study Of The Association Of Genetic Factors With Recovery Of Hypothalamic-Pituitary-Adrenal Axis In Cushing Disease
por: Nguyen, Matthew H, et al.
Publicado: (2023)

Residual manifestations of hypercortisolemia following surgical treatment in a patient with Cushing syndrome
por: Bartz, Sara K., et al.
Publicado: (2015)

SAT-543 Human Hair Aldosterone Measurements for Evaluation of Primary Aldosteronism
por: Demidowich, Andrew Paul, et al.
Publicado: (2020)

Harvey Cushing Treated the First Known Patient With Carney Complex
por: Tsay, Cynthia J., et al.
Publicado: (2017)

ARMC5 Variants and Risk of Hypertension in Blacks: MH‐GRID Study
por: Zilbermint, Mihail, et al.
Publicado: (2019)

SAT-261 Prospective Study of the Association between Early Adrenarche and Cognitive Function in Children with Cushing Disease
por: Keil, Margaret, et al.
Publicado: (2019)

Pituitary adenomas evade apoptosis via noxa deregulation in Cushing’s disease
por: Asuzu, David T., et al.
Publicado: (2022)

OR2802 A Novel CABLES1 Missense Variant Associated With Cushing's Disease Disrupts Protein Structure And Stability
por: Franco-Álvarez, Alexa L, et al.
Publicado: (2023)

SUN-713 Prevalence of Renal Cysts in Patients with Carney Complex
por: Kamilaris, Crystal Dawn Chrysavgi, et al.
Publicado: (2020)

THU478 Unchecked Kinase Activation Underlies Pituitary Adenomas Causing Cushing’s Disease
por: Asuzu, David, et al.
Publicado: (2023)

OR22-07 Novel Variants in Protein Kinase a Signaling-Related Genes Identified in Obese Children with and Without NAFLD
por: Bloyd, Michelle, et al.
Publicado: (2020)

Corticotropinoma as a Component of Carney Complex
por: Hernández-Ramírez, Laura C., et al.
Publicado: (2017)

Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates
por: Korkut, Sabriye, et al.
Publicado: (2016)

High-frequency variants in PKA signaling-related genes within a large pediatric cohort with obesity or metabolic abnormalities
por: Bloyd, Michelle, et al.
Publicado: (2023)

Diabetes-related Bias in Electronic Health Records and International Classification of Diseases
por: Zilbermint, Mihail
Publicado: (2022)

Abnormal Pituitary Imaging and Associated Endocrine Dysfunctions in Erdheim-Chester Disease
por: Shekhar, Skand, et al.
Publicado: (2021)

Molecular Genetic and Genomic Alterations in Cushing’s Syndrome and Primary Aldosteronism
por: Kamilaris, Crystal D. C., et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_gbo91ckn3tvh3gp5hpa63lec8k