Type B diencephalic–mesencephalic junction dysplasia, a congenital brainstem malformation that may be silent until adulthood: a case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s10072-020-04326-4.pdf
Reference5 articles.
1. Zaki MS, Saleem SN, Dobyns WB, Barkovich AJ, Bartsch H, Dale AM, Ashtari M, Akizu N, Gleeson JG, Grijalvo-Perez AM (2012) Diencephalic–mesencephalic junction dysplasia: a novel recessive brain malformation. Brain 135:2416–2427. https://doi.org/10.1093/brain/aws162
2. Madry J, Szlufik S, Koziorowski D, Królicki L (2017) The patient with mild diencephalic–mesencephalic junction dysplasia – case report and review of literature. Neurol Neurochir Pol 51(6):514–518. https://doi.org/10.1016/j.pjnns.2017.08.005
3. Abdel Razek AA, Castillo M (2016) Magnetic resonance imaging of malformations of midbrain-hindbrain. J Comput Assist Tomogr 40(1):14–25. https://doi.org/10.1097/RCT.0000000000000340
4. Barkovich AJ, Millen KJ, Dobyns WB (2007) A developmental classification of malformations of the brainstem. Ann Neurol 62:625–639. https://doi.org/10.1002/ana.21239
5. Severino M, Tortora D, Pistorio A, Ramenghi LA, Napoli F, Mancardi MM, Striano P, Capra V, Rossi A (2016) Expanding the spectrum of congenital anomalies of the diencephalic–mesencephalic junction. Neuroradiology 58(1):33–44. https://doi.org/10.1007/s00234-015-1601-x
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