Cargando…
Congenital adrenal hyperplasia presenting as pelvic inflammatory disease in a phenotypic male: A case report
RATIONALE: Congenital adrenal hyperplasia (CAH) is caused by various enzyme deficiencies, among which 21-hydroxylase (21-OH) deficiency accounts for more than 90% of cases. Neonatal screening became mandatory only a few decades ago. Many patients who were born before this went undiagnosed and some o...
Autores principales: | Lim, Eunsoo, Jeon, Ja Young |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959940/ https://www.ncbi.nlm.nih.gov/pubmed/31914016 http://dx.doi.org/10.1097/MD.0000000000018387 |
Ejemplares similares
-
A case report of pedigree of a homozygous mutation of the steroidogenic acute regulatory protein causing lipoid congenital adrenal hyperplasia
por: Fu, Rong, et al.
Publicado: (2017) -
Adrenal pheochromocytoma presenting with Takotsubo-pattern cardiomyopathy and acute heart failure: A case report and literature review
por: Chiang, Yi-Lun, et al.
Publicado: (2016) -
Pituicytoma Coexisting With Corticotroph Hyperplasia: Literature Review With One Case Report
por: Guo, Xiaopeng, et al.
Publicado: (2016) -
A case report of idiopathic hyperaldosteronism characterized by bilateral adrenal adenoma
por: Wang, Wei, et al.
Publicado: (2019) -
Chronic primary adrenal insufficiency after unilateral adrenonephrectomy: A case report
por: Yoshiji, Satoshi, et al.
Publicado: (2017)