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Amyloid liver
Fatty degeneration of liver
Fatty degeneration of the liver
Fatty liver
Hepatic degeneracy
Lardaceous liver
Lipoid degeneration of the liver
Lipoid liver degeneration
Liver degeneration
Mucoid degeneration
Myxoid degeneration
Myxomatous degeneration
Progressive neuronal degeneration with liver cirrhosis
Waxy liver

Vertaling van "Liver degeneration " (Engels → Frans) :

lipoid liver degeneration

dégénérescence lipoïde du foie


hepatic degeneracy [ liver degeneration ]

dégénérescence hépatique


fatty degeneration of liver | fatty liver

dégénérescence graisseuse du foie | hépatite graisseuse | stéatose hépatique


Lipoid degeneration of the liver

dégénérescence lipoïde


fatty degeneration of the liver

dégénérescence graisseuse du foie


Progressive neuronal degeneration with liver cirrhosis

poliodystrophie sclérosante progressive


mucoid degeneration | myxoid degeneration | myxomatous degeneration

dégénérescence mucoïde | dégénérescence myxomateuse


amyloid liver | lardaceous liver | waxy liver

foie amyloïde | foie cireux | foie lacardé


Spinocerebellar ataxia type 28 (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s

ataxie spinocérébelleuse type 28


A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies

maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante D




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'Liver degeneration' ->

Date index: 2022-06-24
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