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Autosomal dominant Brown–Vialetto–Van Laere syndrome with UBQLN1 mutation

✍ Scribed by Spataro, R.; Conforti, F.L.; Mazzei, R.; La Bella, V.


Book ID
122485973
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
60 KB
Volume
333
Category
Article
ISSN
0022-510X

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Brown-Vialetto-Van Laere syndrome in a l
✍ M�garban�, A.; Desguerres, I.; Rizkallah, E.; Delague, V.; Nabbout, R.; Barois, 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 27 KB 👁 2 views

Brown-Vialetto-Van Laere syndrome or pontobulbar palsy with deafness is a rare disorder characterized by bilateral nerve deafness, a variety of cranial nerve disorders usually involving the motor components of the 7th and 9th to 12th cranial nerves, and less commonly an involvement of spinal motor n