Altered pituitary morphology as a sign of benign hereditary chorea caused by TITF1/NKX2.1 mutations

Benign hereditary chorea (BHC) is a rare genetically heterogeneous movement disorder, in which conventional neuroimaging has been reported as normal in most cases. Cystic pituitary abnormalities and features of empty sella have been described in only 7 patients with BHC to date. We present 4 patient...

Descripción completa

Detalles Bibliográficos
Autores principales: Thust, Steffi, Veneziano, Liana, Parkinson, Michael H., Bhatia, Kailash P., Mantuano, Elide, Gonzalez-Robles, Cristina, Davagnanam, Indran, Giunti, Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960566/
https://www.ncbi.nlm.nih.gov/pubmed/35079915
http://dx.doi.org/10.1007/s10048-021-00680-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960566/
https://www.ncbi.nlm.nih.gov/pubmed/35079915
http://dx.doi.org/10.1007/s10048-021-00680-3

Ejemplares similares