References
Alexander WS. Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant. Brain. 1949;72:373–81.
Garcia L, Gascon G, Ozand P, Yaish H. Increased intracranial pressure in Alexander disease: a rare presentation of white matter disease. J Child Neurol. 1992;7:168–71.
Ozkaya H, Akcan AB, Aydemir G, et al. Juvenile Alexander disease. EAJM. 2012;44:46–50.
Gingold MK, Bodensteiner JB, Schochet SS, Jaynes M. Alexander’s disease: unique presentation. J Child Neurol. 1999;14:325–9.
Lee JM, Kim AS, Lee SJ, et al. A case of infantile Alexander disease accompanied by infantile spasms diagnosed by DNA analysis. J Korean Med Sci. 2006;21:954–7.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Ethical Clearance
Obtained from Institute Ethical committee, Indira Gandhi Institute of Child Health, Bengaluru.
Conflict of Interest
None.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Gowda, V.K., Srinivasan, V.M., Bhat, M. et al. Infantile Alexander Disease Presenting with Hydrocephalus and Epileptic Spasms. Indian J Pediatr 87, 871–872 (2020). https://doi.org/10.1007/s12098-020-03254-7
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s12098-020-03254-7