Cargando…
Compliance Issues in Managing 21 Hydroxylase Deficiency and their Short/Long-Term Consequences
OBJECTIVE: To report a case of untreated classic 21 hydroxylase (OH) deficiency congenital adrenal hyperplasia (CAH) in a transgender patient resulting in pulmonary embolisms (PEs) and bilateral adrenal masses. METHODS: A 36-year-old male (birth sex: female) presenting with bilateral PEs in the sett...
Autores principales: | Lin, Jack, Khoo, Teck K, Voelschow, Erin R, Viets, Zachary J |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SMC Media Srl
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668005/ https://www.ncbi.nlm.nih.gov/pubmed/34912752 http://dx.doi.org/10.12890/2021_003048 |
Ejemplares similares
-
Data on the functional consequences of the mutations identified in 21-Hydroxylase deficient CAH patients
por: Khajuria, Ragini, et al.
Publicado: (2018) -
Impact of Long-Term Dexamethasone Therapy on the Metabolic Profile of Patients With 21-Hydroxylase Deficiency
por: Seraphim, Carlos E, et al.
Publicado: (2019) -
Long-Term Gynecological Outcomes in Women with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
por: Johannsen, T. H., et al.
Publicado: (2010) -
Long term follow up of growth in children with Congenital Adrenal Hyperplasia 21- Hydroxylase deficiency
por: Parikh, Ruchi, et al.
Publicado: (2015) -
Adrenal Morphology as an Indicator of Long-Term Disease Control in Adults with Classic 21-Hydroxylase Deficiency
por: Kim, Taek Min, et al.
Publicado: (2022)