CASE REPORT: HALLERVORDEN-SPATZ SYNDROME WITH SEIZURES

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GOTHWAL SUNIL; NAYAN SWATI

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Journal Paper

Paper Information

Journal: Basic and Clinical Neuroscience Year:2016 | Volume:7 | Issue:2 Page(s): 165-166

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Title

CASE REPORT: HALLERVORDEN-SPATZ SYNDROME WITH SEIZURES

Author(s)

GOTHWAL SUNIL | NAYAN SWATI | Issue Writer Certificate

Keywords

PANTOTHENATE KINASE-ASSOCIATED NEURODEGENERATION

AUTOSOMAL RECESSIVE

SEIZURES

Abstract

Hallervorden-Spatz syndrome is a disorder characterized by dystonia, parkinsonism, and iron accumulation in the brain. The disease is caused by mutations in gene encoding pantothenate kinase 2 (PANK2) and patients have PANTOTHENATE KINASE-ASSOCIATED NEURODEGENERATION. We present an 8-year-old boy with progressive muscle dystonia, neuroregression, frequent fall and multiple injury marks of different stages. SEIZURES are rare with PANK2. This child had seizure onset at 4 years of age and seizure free on valproate and levetricetam. The CT scan showed tiger eye appearance and mutations on PANK2 gene.

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APA: Copy

GOTHWAL, SUNIL, & NAYAN, SWATI. (2016). CASE REPORT: HALLERVORDEN-SPATZ SYNDROME WITH SEIZURES. BASIC AND CLINICAL NEUROSCIENCE, 7(2), 165-166. SID. https://sid.ir/paper/327806/en

Vancouver: Copy

GOTHWAL SUNIL, NAYAN SWATI. CASE REPORT: HALLERVORDEN-SPATZ SYNDROME WITH SEIZURES. BASIC AND CLINICAL NEUROSCIENCE[Internet]. 2016;7(2):165-166. Available from: https://sid.ir/paper/327806/en

IEEE: Copy

SUNIL GOTHWAL, and SWATI NAYAN, “CASE REPORT: HALLERVORDEN-SPATZ SYNDROME WITH SEIZURES,” BASIC AND CLINICAL NEUROSCIENCE, vol. 7, no. 2, pp. 165–166, 2016, [Online]. Available: https://sid.ir/paper/327806/en

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