Cargando…
Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesis
BACKGROUND: Congenital adrenal hyperplasia (CAH) is an inherited recessive disorder of adrenal steroidogenesis. The enzymes most commonly affected are 21-hydroxylase. Past reports suggested brain magnetic resonance imaging (MRI) abnormalities in CAH patients, affecting white matter signal, temporal...
Autores principales: | Mnif, Mouna Feki, Kamoun, Mahdi, Mnif, Fatma, Charfi, Nadia, Kallel, Nozha, Rekik, Nabila, Naceur, Basma Ben, Fourati, Hela, Daoud, Emna, Mnif, Zainab, Sfar, Mohamed Habib, Younes-Mhenni, Samia, Sfar, Mohamed Tahar, Hachicha, Mongia, Abid, Mohamed |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659878/ https://www.ncbi.nlm.nih.gov/pubmed/23776864 http://dx.doi.org/10.4103/2230-8210.107833 |
Ejemplares similares
-
Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
por: Mnif, Mouna Feki, et al.
Publicado: (2012) -
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) -
Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency
por: Mnif, Mouna Feki, et al.
Publicado: (2013) -
Isolated adrenocorticotropic hormone deficiency due to probable lymphocytic hypophysitis in a woman
por: Kacem, Faten Hadj, et al.
Publicado: (2013) -
Hyperthyroidism: A rare cause of pulmonary embolism: Report of two cases
por: Grine, Sonia, et al.
Publicado: (2013)