Paramagnetic Signals in the Globus Pallidus as Late Radiographic Sign of Juvenile-Onset GM1 Gangliosidosis

被引:9
|
作者
Takenouchi, Toshiki [1 ]
Kosaki, Rika [2 ]
Nakabayashi, Kazuhiko [3 ]
Hata, Kenichiro [3 ]
Takahashi, Takao [1 ]
Kosaki, Kenjiro [4 ]
机构
[1] Keio Univ, Sch Med, Dept Pediat, Tokyo, Japan
[2] Natl Ctr Child Hlth & Dev, Div Med Genet, Tokyo, Japan
[3] Natl Ctr Child Hlth & Dev, Dept Maternal Fetal Biol, Tokyo, Japan
[4] Keio Univ, Sch Med, Ctr Genet Med, Tokyo 1608582, Japan
关键词
GM1; gangliosidosis; GLB1; neurodegeneration with brain iron accumulation; next-generation sequencing;
D O I
10.1016/j.pediatrneurol.2014.09.022
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND: The juvenile form of GM1 gangliosidosis lacks specific physical findings and thus is often a diagnostic challenge for clinicians. T-2 hypodensity in the globus pallidus is a characteristic radiographic sign of neurodegeneration with iron accumulation in the brain that is observed in GM1 gangliosidosis, but the exact timing when this radiographic sign becomes apparent remains to be elucidated. PATIENTS: Two male siblings had normal development until 2 years of age and then developed psychomotor regression with dystonia. Their neuroimaging studies indicated progressive global cerebral atrophy. Exome sequencing identified compound heterozygous missense mutations in GLB1, leading to a diagnosis of GM1 gangliosidosis. RESULTS: A retrospective review of neuroimaging studies revealed that the two patients had strikingly similar clinical courses and radiographic progressions with cortical atrophy that preceded the T-2 hypointensity in the globus pallidus. CONCLUSIONS: Paramagnetic signals in the globus pallidus become apparent relatively late during the disease course, once cerebral atrophy has already become prominent. A comprehensive diagnostic approach involving clinical, radiographic, and genetic testing is necessary for the early identification of affected individuals.
引用
收藏
页码:226 / 229
页数:4
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