A rare genetic central nervous system malformation syndrome characterized by bilateral congenital cataracts and severe hemorrhagic destruction of the brain parenchyma with associated massive cystic degeneration, enlarged ventricles and subependymal c

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

porencefalie, microcefalie, bilateraal congenitaal cataract-syndroom

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Definition: Gradual in onset, following a number of transient ischaemic episodes which produce an accumulation of infarcts in the cerebral parenchyma. | Predominantly cortical dementia

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Omschrijving: Heeft een geleidelijk begin, volgend op een aantal voorbijgaande ischemische episoden die een opeenhoping van infarcten in het hersenparenchym veroorzaken. | Neventerm: | overwegend corticale dementie

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Tumor of lung parenchyma

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neoplasma van longparenchym

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Entire lung parenchyma

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volledig longparenchym

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Anderen hebben gezocht naar : entire lung parenchyma predominantly cortical dementia tumor of lung parenchyma axial parenchyma diffuse-zonate parenchyma functional tissue of an organ longitudinal parenchyma parenchyma vertical parenchyma wood parenchyma xylem parenchyma

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'xylem parenchyma' ->

Date index: 2024-02-12