Cargando…

Are Current Normal Values of 11DOC Useful for Diagnosis of Non Classical Congenital Adrenal Hyperplasia Due to 11β- Hydroxylase Deficiency?

Background: A non-classic form of 11β-hydroxylase deficiency (NC 11β-OHD) has been reported to cause mild androgen excess, with a clinical presentation of precocious puberty, menstrual cycle abnormalities, or hirsutism during adolescence. Since genetic diagnosis of NC 11βOHD is yet not routinely ava...

Descripción completa

Detalles Bibliográficos
Autores principales:	Barash, Galia, Drach, Lior, Naugolni, Larisa, Yacoel, Tamar, Bistritzer, Tzvi Tzvi, Rachmiel, Marianna
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2021
Materias:	Pediatric Endocrinology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090501/ http://dx.doi.org/10.1210/jendso/bvab048.1444

Ejemplares similares

THU207 11-oxygenated Androgens Are Strongly Associated With Treatment Quality In Children With Congenital Adrenal Hyperplasia Due To 21-Hydroxylase Deficiency
por: Abawi, Ozair, et al.
Publicado: (2023)

Height augmentation in 11β-hydroxylase deficiency congenital adrenal hyperplasia
por: Nour, Munier A, et al.
Publicado: (2015)

Gender identity in congenital adrenal hyperplasia secondary to 11-hydroxylase deficiency
por: Bin-Abbas, Bassam S., et al.
Publicado: (2006)

Testicular Adrenal Rest Tumor in 11-Beta-Hydroxylase Deficiency Driven Congenital Adrenal Hyperplasia
por: Kaynar, Mehmet, et al.
Publicado: (2014)

Phenotype of patients with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
por: Dung, Vu Chi, et al.
Publicado: (2015)

SUN-LB11 What Is the Value of Clinical Suspicion in Neonatal Screening for Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency (CAH 21OHD)?
por: Fernández, María Sanz, et al.
Publicado: (2020)

Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency in a Tunisian family
por: Elfekih, Hamza, et al.
Publicado: (2020)

Clinical and Molecular Analysis of Four Patients With 11β-Hydroxylase Deficiency
por: Zhou, Qiaoli, et al.
Publicado: (2020)

Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany
por: Dörr, Helmuth G., et al.
Publicado: (2018)

Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency
por: Dörr, Helmuth G., et al.
Publicado: (2018)

Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia
por: Righi, Beatrice, et al.
Publicado: (2023)

SUN-071 Prenatal and Post-Natal Influence of Androgens in the Psychosexual Development in Individuals with 21-hydroxylase Congenital Adrenal Hyperplasia
por: Batista, Rafael Loch, et al.
Publicado: (2020)

A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy
por: Alqahtani, Mohammad A., et al.
Publicado: (2015)

Leydig Cell Tumor Associated with Testicular Adrenal Rest Tumors in a Patient with Congenital Adrenal Hyperplasia due to 11β-Hydroxylase Deficiency
por: Charfi, Nadia, et al.
Publicado: (2012)

Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: description of a new mutation, R384X
por: Matallana-Rhoades, Audrey Mary, et al.
Publicado: (2016)

Editorial: Management of Females with Congenital Adrenal Hyperplasia
por: González, Ricardo, et al.
Publicado: (2017)

Comparison of different glucocorticoid regimens in the management of classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
por: Ajish, T. P., et al.
Publicado: (2014)

Congenital Adrenal Hyperplasias Presenting in the Newborn and Young Infant
por: Balsamo, Antonio, et al.
Publicado: (2020)

SUN-281 Topiramate-Induced BMI Reduction in an Adolescent with Severe Obesity Associated with Classical Congenital Adrenal Hyperplasia
por: Seagroves, Amy, et al.
Publicado: (2019)

Long-Term Health Outcomes of Korean Adults With Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
por: Lim, Seung Gyun, et al.
Publicado: (2021)

Characteristics of Growth in Children With Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency During Adrenarche and Beyond
por: Troger, Tobias, et al.
Publicado: (2021)

Malaysian Females With Congenital Adrenal Hyperplasia: Surgical Outcomes and Attitudes
por: Zainuddin, Ani Amelia, et al.
Publicado: (2019)

Male Gender Identity and Reversible Hypokalemic Hypertension in a 46,XX Child with 11-Beta-Hydroxylase Deficiency Congenital Adrenal Hyperplasia
por: Goyal, Alpesh, et al.
Publicado: (2019)

OR18-4 Crinecerfont (NBI-74788), a Novel CRF1 Receptor Antagonist, Lowers Adrenal Androgens and Precursors in Adolescents with Classic Congenital Adrenal Hyperplasia
por: Auchus, Richard, et al.
Publicado: (2022)

Treatment and Outcome of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
por: Lee, Peter A., et al.
Publicado: (2010)

The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
por: Pignatelli, Duarte, et al.
Publicado: (2019)

11-Oxygenated Androgens Are Biomarkers of Adrenal Volume and Testicular Adrenal Rest Tumors in 21-Hydroxylase Deficiency
por: Turcu, Adina F., et al.
Publicado: (2017)

Blood Pressure and Left Ventricular Characteristics in Young Patients with Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
por: Ubertini, Graziamaria, et al.
Publicado: (2009)

Classic Congenital Adrenal Hyperplasia Due To 21-hydroxylase Deficiency – the Next Disease Included in The Neonatal Screening Program in Poland
por: Ginalska-Malinowska, Maria
Publicado: (2018)

SAT358 Race And Ethnicity Of Women With 21-hydroxylase Deficient Non-classic Adrenal Hyperplasia (NCAH) Compared With PCOS
por: Pace, Lauren Arielle, et al.
Publicado: (2023)

SAT-286 A Previously Undescribed Combination of Aromatase Deficiency and Non-Classical Congenital Adrenal Hyperplasia in an Hispanic Teenage Male
por: Gottesman, Bethany, et al.
Publicado: (2019)

Referrals and Management Strategies for Pediatric Obesity—DocStyles Survey 2017
por: Imoisili, Omoye E., et al.
Publicado: (2018)

SAT-LB067 Mutational Spectrum Determines Subtle Adrenal Biosynthetic Defect in Non-Classical Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
por: Mermejo, Livia, et al.
Publicado: (2019)

Adrenal Tumor Mimicking Non-Classic Congenital Adrenal Hyperplasia
por: Tsai, Wen-Hsuan, et al.
Publicado: (2020)

MON-LB049 Central Precocious Puberty as a Presenting Sign of Non-Classical Congenital Adrenal Hyperplasia: Prevalence and Clinical Characteristics
por: de Vries, Liat, et al.
Publicado: (2019)

THU187 Genotype-Phenotype Correlation, Clinical Presentation And Feminizing Surgery In Children With Congenital Adrenal Hyperplasia Due To 21-Hydroxylase Deficiency: A Nationwide Multi-Center Study
por: Lind-Holst, Marie, et al.
Publicado: (2023)

Pitfalls in molecular diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia
por: Kolahdouz, Mahsa, et al.
Publicado: (2015)

Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
por: Pignatelli, Duarte, et al.
Publicado: (2020)

An Evidence-Based Model of Multidisciplinary Care for Patients and Families Affected by Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
por: Schaeffer, Traci L., et al.
Publicado: (2010)

Non-Classical Congenital Adrenal Hyperplasia in Childhood
por: Kurtoğlu, Selim, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_1813832jnmlhc7djmhqb0dq1j0