| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) |
| HTRA1-related autosomal dominant cerebral small vessel disease |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease
HTRA1-related autosomal dominant cerebral angiopathy
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| A rare genetic cerebral small vessel disease characterized by subcortical ischemic events associated with cognitive decline and gait disturbance with an age of onset typically in the sixth or seventh decade of life. Imaging reveals white matter hyperintensities, status cribrosum, lacunar infarcts and sometimes microbleeds. Extra-neurological manifestations are absent. |
| HTRA1-gerelateerde autosomaal dominante 'cerebral small vessel disease' |
| 'HtrA serine peptidase 1'-gerelateerde autosomaal dominante 'cerebral small vessel disease'
HTRA1-gerelateerde autosomaal dominante CSVD
HTRA1-gerelateerde autosomaal dominante ziekte van kleine hersenvaten
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