| cerebrohepatorenal s. |
an autosomal recessive disorder characterized by craniofacial abnormalities, hypotonia, hepatomegaly, polycystic kidneys, jaundice, and death in early infancy, and associated with absence of peroxisomes in the liver and kidneys; called also Zellweger s.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| cerebroid |
resembling the cerebral substance.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| cerebrology |
the sum of knowledge regarding cerebral structure and function.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| cerebromacular |
maculocerebral.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| cerebromacular d. |
1. degeneration of brain cells and the macula luteae, as in Tay-Sachs disease. 2. any lipidosis with cerebral lesions and degeneration of the retinal macula. 3. any form of neuronal ceroid-lipofuscinosis.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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