Lhermitte-Duclos disease with concomitant KCNT2 gene mutation: report of an extremely rare combination
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00381-023-06039-3.pdf
Reference12 articles.
1. Pregúntegui-Loayza I, Apaza-Tintaya A, Ramírez-Espinoza A, Mayo-Simón N, Toledo-Aguirre M (2021) Lhermitte-Duclos disease in pediatric population: report of 2 cases. Pediatr Neurosurg 56(3):279–285
2. Dietlein M, Schröder R, Widemann B, Benz-Bohm G (1992) Dysplastic gangliocytoma of cerebellum in a newborn. Diagnosis by ultrasonography and MRI. Pediatr Radiol 22(2):131–133
3. Jiang T, Wang J, Du J, Luo S, Liu R, Xie J, Wang Y, Li C (2017) Lhermitte-Duclos disease (dysplastic gangliocytoma of the cerebellum) and Cowden syndrome: clinical experience from a single institution with long-term follow-up. World Neurosurg 104:398–406
4. Robinson S, Cohen AR (2006) Cowden disease and Lhermitte-Duclos disease: an update. Case report and review of the literature. Neurosurg Focus 20(1):E6
5. Roessmann U, Wongmongkolrit T (1984) Dysplastic gangliocytoma of cerebellum in a newborn. Case report J Neurosurg 60(4):845–847
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