Vertaling van "coagulation disorder " (Engels → Nederlands) :

coagulation disorder
stoornissen in de bloedstolling

person with coagulation disorders
persoon met coagulatie-stoornissen

Purpura with coagulation disorder
purpura van huid en/of mucosa gelijktijdig met en door stollingsstoornis

hereditary disorder affecting coagulation of blood
erfelijke stoornis in de bloedstolling

coagulation tank tending | operate coagulation tanks | coagulation tanks operating | tend coagulation tanks
coagulatietanks bedienen | stollingstanks bedienen

latex coagulation operative | rubber coagulation operative | coagulation operator | latex coagulation operator
operator gemalen rubber | allround operator chemische industrie | operator rubberproductie

develop a long-term treatment course for disorders in the glandular system | establish a long-term treatment plan for disorders of the glandular system | develop long-term treatment course for disorders in the glandular system | lay out long-term treatment course for disorders in the glandular system
langetermijnbehandelingen ontwikkelen voor aandoeningen aan het kliersysteem

A rare congenital bleeding disorder resulting from variably decreased levels of coagulation factors II, VII, IX and X, as well as natural anticoagulants protein C, protein S and protein Z. Other symptoms are often present, including developmental and
erfelijke gecombineerde deficiëntie van vitamine K-afhankelijke stollingsfactoren

Glomerular disorders in:cryoglobulinaemia (D89.1+) | disseminated intravascular coagulation [defibrination syndrome] (D65+) | haemolytic-uraemic syndrome (D59.3+) | Henoch(-Schönlein) purpura (D69.0+) | sickle-cell disorders (D57.-+)
glomerulaire aandoeningen bij | cryoglobulinemie (D89.1) | glomerulaire aandoeningen bij | gedissemineerde intravasale stolling [defibrinatiesyndroom] (D65) | glomerulaire aandoeningen bij | hemolytisch-uremisch syndroom (D59.3) | glomerulaire aandoeningen bij | purpura van Henoch(-Schönlein) (D69.0) | glomerulaire aandoeningen bij | sikkelcelaandoeningen (D57.-)

A congenital disorder of glycosylation with characteristics of macrocephaly due to Dandy-Walker malformation, hydrocephaly, hypotonia, myopathy and coagulation anomalies. To date, only one case has been reported. The syndrome is associated with mutat
congenitaal defect in glycosylering type IId