Cargando…

Diagnosis and prevalence of Congenital Adrenal Hyperplasia (CAH) in Austrian children screened or not screened for CAH

Detalles Bibliográficos
Autores principales:	Luxenberger, Katharina, Kasper, David, Fröhlich-Reiterer, Elke, Suppan, Elisabeth, Weinhandl, Gudrun, Borkenstein, Martin
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2013
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850226/ http://dx.doi.org/10.1186/1687-9856-2013-S1-P111

Ejemplares similares

Prevalence of CAH-X Syndrome in Italian Patients with Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency
por: Paragliola, Rosa Maria, et al.
Publicado: (2022)

Comprehensive and Cost-Effective Strategy for Genetic Screening of Congenital Adrenal Hyperplasia (CAH) in India
por: Ravichandran, Lavanya, et al.
Publicado: (2021)

Thirty-Year Lessons from the Newborn Screening for Congenital Adrenal Hyperplasia (CAH) in Japan
por: Tsuji-Hosokawa, Atsumi, et al.
Publicado: (2021)

Case Report of an Adult Female with Neglected Congenital Adrenal Hyperplasia (CAH)
por: Krishnan, Gayathri Devi, et al.
Publicado: (2018)

Pitfalls of Prenatal Diagnosis guiding Postnatal Management in Congenital Adrenal Hyperplasia(CAH)
por: Murthy, Deepa Badrinath, et al.
Publicado: (2021)

Tackling “pillar 5” – exploring options to help families of children who are living with congenital adrenal hyperplasia (CAH) in Vietnam to achieve financial independence
por: Armstrong, KL, et al.
Publicado: (2013)

Testicular Adrenal Rest Tumors (TARTS) With Unusual Histological Features in Congenital Adrenal Hyperplasia (CAH)
por: Marianovsky, Valeri, et al.
Publicado: (2015)

MON-177 CAH-X Syndrome in a German Cohort of Patients with Congenital Adrenal Hyperplasia
por: Sappl, Andrea, 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)

Congenital Adrenal Hyperplasia (CAH) and Gitelman Syndrome (GS): Overlapping Symptoms in an Uncommon Association
por: Calcaterra, Valeria, et al.
Publicado: (2021)

Newborn Screening for CAH—Challenges and Opportunities
por: Heather, Natasha L., et al.
Publicado: (2021)

Is It Beneficial to Patients to Include Congenital Adrenal Hyperplasia (CAH) Among the Disorders of Sex Development (DSD)?
por: González, Ricardo, et al.
Publicado: (2018)

Early Feminizing Genitoplasty in Girls with Congenital Adrenal Hyperplasia (CAH)—Analysis of Unified Surgical Management
por: Kudela, Grzegorz, et al.
Publicado: (2020)

The Burden of Illness of Congenital Adrenal Hyperplasia (CAH) in Adults: Results: of a Structured Literature Review
por: Woods, Matthew Stephen, et al.
Publicado: (2021)

ODP394 Prevalence of Anxiety and Depressive Symptoms in Children and Adolescents with Congenital Adrenal Hyperplasia (CAH)
por: Jacob, Marianne, et al.
Publicado: (2022)

CAH Newborn Screening in India: Challenges and Opportunities
por: Dabas, Aashima, et al.
Publicado: (2020)

Physical, social and societal functioning of children with congenital adrenal hyperplasia (CAH) and their parents, in a Dutch population
por: Sanches, Sarita A, et al.
Publicado: (2012)

SUN-167 Treatment Considerations for a Healthy Pregnancy in Women with Classical Congenital Adrenal Hyperplasia (CAH)
por: Calzia, Megan, et al.
Publicado: (2020)

SUN-172 A False Positive Result in Newborn Screening for Congenital Adrenal Hyperplasia (CAH) in a Girl with Beckwith Wiedemann Syndrome
por: Braga, Barbara Leitao, et al.
Publicado: (2020)

SUN-197 Giant Adrenal Myelolipoma Associated with Prolonged ACTH Elevation in a Patient with Congenital Adrenal Hyperplasia (CAH)
por: Kaluarachchi, Vidumini, et al.
Publicado: (2020)

Diagnosis and management of rare forms of CAH
por: Sahakitrungruang, Taninee
Publicado: (2015)

Evaluation of parental knowledge after establishing CAH clubs in Vietnam & Indonesia
por: Mitchelhill, Irene, et al.
Publicado: (2015)

PSAT095 Examination of Treatment Patterns in Patients with Classic Congenital Adrenal Hyperplasia (CAH) Compared to Treatment Guidelines
por: Manahan, Rachel, et al.
Publicado: (2022)

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)

Molecular genetic testing of congenital adrenal hyperplasia due to 21-hydroxylase deficiency should include CAH-X chimeras
por: Lao, Qizong, et al.
Publicado: (2021)

Growth and Metabolic Syndrome (MetS) Criteria in Young Children with Classic Congenital Adrenal Hyperplasia (CAH) Treated with Corticosteroids (CS)
por: Abdel Meguid, Shaymaa Elsayed, et al.
Publicado: (2022)

Manuscrito de Chan Cah.
Publicado: (1982)

Long-term prednisone versus hydrocortisone treatment in children with classic congenital adrenal hyperplasia (CAH) and a brief review of the literature
por: Ahmed, Shaymaa Elsayed Abdel Meguid, et al.
Publicado: (2019)

RF09 | PSAT70 Comparison of Prednisolone Versus Modified-release Hydrocortisone (Efmody) in the Treatment of Congenital Adrenal Hyperplasia (CAH)
por: Merke, Deborah P, et al.
Publicado: (2022)

MON-170 Real World Estimates of Adrenal Insufficiency Related Adverse Events in Children with Congenital Adrenal Hyperplasia: On Behalf of the I-CAH Consortium
por: Ali, Salma R, et al.
Publicado: (2020)

The etiology and clinical features of non-CAH primary adrenal insufficiency in children
por: Liu, Ziqin, et al.
Publicado: (2022)

FRI245 Non-classic CAH Presenting As Bilateral Adrenal Incidentalomas
por: Chin, Yun Ann, et al.
Publicado: (2023)

Two cases of male patients followed for a classical form of congenital adrenal hyperplasia (CAH), presenting an azoospermia: analysis and review of the literature
por: Fouques, Clélia, et al.
Publicado: (2019)

Measurement of serum tenascin-X in patients with congenital adrenal hyperplasia at risk for Ehlers–Danlos contiguous gene deletion syndrome CAH-X
por: Kolli, Vipula, et al.
Publicado: (2019)

Health status of children and young persons with congenital adrenal hyperplasia in the UK (CAH-UK): a cross-sectional multi-centre study
por: Bacila, Irina, et al.
Publicado: (2022)

Should CAH in Females Be Classified as DSD?
por: González, Ricardo, et al.
Publicado: (2016)

Unusual Combination of MEN-1 and the Contiguous Gene Deletion Syndrome of CAH and Ehlers-Danlos Syndrome (CAH-X)
por: Chen Cardenas, Stanley M, et al.
Publicado: (2020)

Tildacerfont for the Treatment of Patients With Classic Congenital Adrenal Hyperplasia: Results From a 12-Week Phase 2 Clinical Trial in Adults With Classic CAH
por: Auchus, Richard Joseph, et al.
Publicado: (2021)

Hospital Admission Patterns in Children with CAH: Admission Rates and Adrenal Crises Decline with Age
por: Rushworth, R. Louise, et al.
Publicado: (2016)

SAT326 Massive Adrenomyelolipomas Due To Longstanding CAH
por: Aziz, Qurrat-ul-ain, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_o4go7hkk91k8m627hoj37589f0