Probable Vanishing White Matter Disease: A Case Report and Literature Review

被引:5
作者
Deginet, Endayen [1 ]
Tilahun, Robel [2 ]
Bishaw, Solomon [3 ]
Eshetu, Konjit [2 ]
Moges, Ayalew [4 ]
机构
[1] Dire Dawa Univ, Coll Hlth Sci, Sch Med, Dept Pediat & Child Hlth, Dire Dawa, Ethiopia
[2] Haramaya Univ, Coll Hlth Sci, Sch Med, Dept Pediat & Child Hlth, Harar, Ethiopia
[3] Haramaya Univ, Coll Hlth Sci, Dept Radiol, Harar, Ethiopia
[4] Addis Ababa Univ, Coll Hlth Sci, Sch Med, Dept Pediat & Child Hlth, Addis Ababa, Ethiopia
关键词
Vanishing White Matter Disease; Child; Ethiopia;
D O I
10.4314/ejhs.v31i6.28
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
BACKGROUND: Vanishing white matter disease is one of the most prevalent inherited childhood leukoencephalopathies. The disease is characterized by chronic, progressive and episodic deterioration with ataxia and spasticity. CASE PRESENTATION: Here, we report a 15-month-old female child from Dire-Dawa, eastern part of Ethiopia, who presented with regression of developmental milestones and truncal ataxia since her age of 11 months following a febrile illness that occurred one month earlier. Magnetic resonance imaging of brain is suggestive of vanishing white matter disease. CONCLUSIONS: We believe this case report will increase curiosity, awareness and knowledge of health professionals in Ethiopia and sub-Saharan Africa working with children in early consideration and the diagnosis of the disease.
引用
收藏
页码:1307 / 1310
页数:4
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