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Case Report: Subacute Sclerosing Panencephalitis Presenting as Acute Encephalitis.
Am J Trop Med Hyg. 2019 07; 101(1):260-262.AJ

Abstract

Subacute sclerosing panencephalitis (SSPE) is still a common disease in India which is characterized by a progressive mental decline, myoclonus, periodic encephalographic abnormalities, and raised anti-measles antibody titter in the cerebrospinal fluid. Acute fulminant SSPE is characterized by a rapid course of disease culminating in death, within 6 months. We report of a 10-year-old boy, who came with a 14-day history of continuous involuntary jerky movements of the left half of the body, including the head. There was a highly increased anti-measles IgG antibody titer, both in the cerebrospinal fluid and serum. We conclude that acute rapidly progressive SSPE can present as acute encephalitis syndrome.

Authors+Show Affiliations

Department of Neurology, King George's Medical University, Lucknow, India.Department of Neurology, King George's Medical University, Lucknow, India.Department of Neurology, King George's Medical University, Lucknow, India.Department of Microbiology, King George's Medical University, Lucknow, India.Department of Neurology, King George's Medical University, Lucknow, India.Department of Neurology, King George's Medical University, Lucknow, India.Department of Neurology, King George's Medical University, Lucknow, India.Department of Microbiology, King George's Medical University, Lucknow, India.Department of Neurology, King George's Medical University, Lucknow, India.

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

31134883

Citation

Garg, Ravindra Kumar, et al. "Case Report: Subacute Sclerosing Panencephalitis Presenting as Acute Encephalitis." The American Journal of Tropical Medicine and Hygiene, vol. 101, no. 1, 2019, pp. 260-262.
Garg RK, Kumar N, Rizvi I, et al. Case Report: Subacute Sclerosing Panencephalitis Presenting as Acute Encephalitis. Am J Trop Med Hyg. 2019;101(1):260-262.
Garg, R. K., Kumar, N., Rizvi, I., Jain, A., Jaipuriar, R. S., Sharma, P. K., Malhotra, H. S., Nasar Khan, D., & Uniyal, R. (2019). Case Report: Subacute Sclerosing Panencephalitis Presenting as Acute Encephalitis. The American Journal of Tropical Medicine and Hygiene, 101(1), 260-262. https://doi.org/10.4269/ajtmh.19-0215
Garg RK, et al. Case Report: Subacute Sclerosing Panencephalitis Presenting as Acute Encephalitis. Am J Trop Med Hyg. 2019;101(1):260-262. PubMed PMID: 31134883.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Case Report: Subacute Sclerosing Panencephalitis Presenting as Acute Encephalitis. AU - Garg,Ravindra Kumar, AU - Kumar,Neeraj, AU - Rizvi,Imran, AU - Jain,Amita, AU - Jaipuriar,Ravi Shekhar, AU - Sharma,Praveen Kumar, AU - Malhotra,Hardeep Singh, AU - Nasar Khan,Danish, AU - Uniyal,Ravi, PY - 2019/5/29/pubmed PY - 2020/1/22/medline PY - 2019/5/29/entrez SP - 260 EP - 262 JF - The American journal of tropical medicine and hygiene JO - Am J Trop Med Hyg VL - 101 IS - 1 N2 - Subacute sclerosing panencephalitis (SSPE) is still a common disease in India which is characterized by a progressive mental decline, myoclonus, periodic encephalographic abnormalities, and raised anti-measles antibody titter in the cerebrospinal fluid. Acute fulminant SSPE is characterized by a rapid course of disease culminating in death, within 6 months. We report of a 10-year-old boy, who came with a 14-day history of continuous involuntary jerky movements of the left half of the body, including the head. There was a highly increased anti-measles IgG antibody titer, both in the cerebrospinal fluid and serum. We conclude that acute rapidly progressive SSPE can present as acute encephalitis syndrome. SN - 1476-1645 UR - https://www.unboundmedicine.com/medline/citation/31134883/Case_Report:_Subacute_Sclerosing_Panencephalitis_Presenting_as_Acute_Encephalitis_ DB - PRIME DP - Unbound Medicine ER -