Adult-onset Alexander’s disease is a rare leukodystrophy that can present later in life in a variety of ways, often mimicking more common neurodegenerative conditions. We present two cases with novel mutations, diagnosed from their characteristic MR scan findings. Even in much older people, clinicians should have a high clinical suspicion if there are typical imaging findings
Alexander Disease is a rare, often fatal, leukoencephalopathy of early childhood associated with a h...
BACKGROUND AND PURPOSE: To date, the demonstration of Rosenthal fibers on brain biopsy or autopsy sp...
Alexander disease (AxD) is a leukodystrophy that primarily affects astrocytes and is caused by domin...
practneurol-2015-001144 Adult-onset Alexander’s disease is a rare leukodystrophy that can present la...
Adult-onset Alexander's disease is a rare leukodystrophy that can present later in life in a variety...
The case describes a 25-year-old Caucasian female diagnosed with Alexander’s disease (AxD) as an out...
BACKGROUND AND PURPOSE: In recent years, the discovery that mutations in the glial fibrillary acidic...
Alexander disease is a rare leukodystrophy that most often presents in infancy but also includes neo...
Alexander disease (AD) in its typical form is an infantile lethal leucodystrophy, characterized path...
Alexander disease is a leukodystrophy caused by dominant missense mutations in the gene encoding the...
Alexander Disease (ALXDRD) is an autosomal dominant leukodystrophy caused by mutation in one allele ...
Leukodystrophies are genetically determined white matter disorders. Even though leukodystrophies ess...
BACKGROUND AND PURPOSE: To date, the demonstration of Rosenthal fibers on brain biopsy or autopsy sp...
Background: Alexander disease (AD) is a sporadic leukodystrophy that predominantly affects infants a...
biopsy or autopsy specimens is considered a prerequisite for a definitive diagnosis of Alexander dis...
Alexander Disease is a rare, often fatal, leukoencephalopathy of early childhood associated with a h...
BACKGROUND AND PURPOSE: To date, the demonstration of Rosenthal fibers on brain biopsy or autopsy sp...
Alexander disease (AxD) is a leukodystrophy that primarily affects astrocytes and is caused by domin...
practneurol-2015-001144 Adult-onset Alexander’s disease is a rare leukodystrophy that can present la...
Adult-onset Alexander's disease is a rare leukodystrophy that can present later in life in a variety...
The case describes a 25-year-old Caucasian female diagnosed with Alexander’s disease (AxD) as an out...
BACKGROUND AND PURPOSE: In recent years, the discovery that mutations in the glial fibrillary acidic...
Alexander disease is a rare leukodystrophy that most often presents in infancy but also includes neo...
Alexander disease (AD) in its typical form is an infantile lethal leucodystrophy, characterized path...
Alexander disease is a leukodystrophy caused by dominant missense mutations in the gene encoding the...
Alexander Disease (ALXDRD) is an autosomal dominant leukodystrophy caused by mutation in one allele ...
Leukodystrophies are genetically determined white matter disorders. Even though leukodystrophies ess...
BACKGROUND AND PURPOSE: To date, the demonstration of Rosenthal fibers on brain biopsy or autopsy sp...
Background: Alexander disease (AD) is a sporadic leukodystrophy that predominantly affects infants a...
biopsy or autopsy specimens is considered a prerequisite for a definitive diagnosis of Alexander dis...
Alexander Disease is a rare, often fatal, leukoencephalopathy of early childhood associated with a h...
BACKGROUND AND PURPOSE: To date, the demonstration of Rosenthal fibers on brain biopsy or autopsy sp...
Alexander disease (AxD) is a leukodystrophy that primarily affects astrocytes and is caused by domin...