Leukodystrophy with premature ovarian failure: think on vanishing white matter disease (VWMD).
نویسندگان
چکیده
A 46-year-old female presented progressive hand tremor at age of 8, associated to cognitive and motor deterioration. She developed incapacitating head tremor and was wheelchair-bound 12 years after onset. Premature ovarian failure (POF) occurred at 27-year-old. In the last 3 years, head tremor became less intense, but she remained with horizontal bidireccional nistagmus. Vanishing white matter disease (VWMD) is an autosomal recessive disorder characterized by cerebellar ataxia, spasticity, and cognitive impairment. Brain MRI discloses symmetric and diffuse white matter lesions ( figure). VWMD manifests from infancy to adulthood; in female, POF may occur. It is caused by mutations in both alleles of one of five genes coding for subunits of eukaryotic translation initiation factor 2B.
منابع مشابه
Vanishing white matter in Saudi Arabia.
Vanishing white matter disease (VWMD) is an under-diagnosed condition that affects the brains white matter at all ages, especially in the pediatric age group. It belongs to a clinically and genetically heterogeneous group of disorders, collectively known as eukaryotic initiation factor 2B-related disorders. The disorder has been described in different ethnic groups. Here, we describe a case of ...
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Vanishing white matter disease (VWMD) is an inherited autosomal-recessive hypomyelinating disease caused by mutations in eukaryotic translation initiation factor 2B (eIF2B). eIF2B mutations predominantly affect the brain white matter, and the characteristic features of VWMD pathology include myelin loss and foamy oligodendrocytes. Activation of pancreatic endoplasmic reticulum kinase (PERK) has...
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ورودعنوان ژورنال:
- Arquivos de neuro-psiquiatria
دوره 73 1 شماره
صفحات -
تاریخ انتشار 2015