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Anomaly
Hereditary leukocytic hypersegmentation
Hyposegmentation
Leukomelanopathy
May-Hegglin
Nuclear anomaly
Pelger nuclear anomaly
Pelger-Huet anomaly
Pelger-Huët

Traduction de «Pelger nuclear anomaly » (Anglais → Néerlandais) :







Anomaly (granulation)(granulocyte) or syndrome:Alder | May-Hegglin | Pelger-Huët | Hereditary:leukocytic:hypersegmentation | hyposegmentation | leukomelanopathy

anomalie (granulatie)(granulocyt) of syndroom van | Alder | anomalie (granulatie)(granulocyt) of syndroom van | May-Hegglin | anomalie (granulatie)(granulocyt) of syndroom van | Pelger-Huët | hereditaire | leukocytaire | hypersegmentatie | hereditaire | leukocytaire | hyposegmentatie | hereditaire | leukomelanopathie


A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterised by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with

progressieve externe oftalmoplegie, myopathie, emaciatie


Retinal dystrophy with inner nuclear layer and ganglion cell anomalies

retinale dystrofie met binnenste retinale disfunctie en ganglioncelanomalieën




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'Pelger nuclear anomaly' ->

Date index: 2023-09-22
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