Примери за използване на Severe congenital на Английски и техните преводи на Български
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Usually severe congenital kyphosis deformity surgery heals.
It's hard to predict which babies will experience severe congenital CVM.
In children and adults with severe congenital, cyclic, or idiopathic neutropenia with an absolute.
What is happening with Ceprotin for the treatment of patients with severe congenital protein C deficiency?
With moderate to severe congenital ptosis, the child may need treatment to have his or her vision develop normally.
By the way, infections threaten not only an early miscarriage, butthe birth of a child with severe congenital diseases.
If CEPROTIN is used in patients with severe congenital protein C deficiency, antibodies inhibiting protein C may develop.
Large populations andall birth outcomes are essential in epidemiological studies of rare and severe congenital anomalies.
If the preparation is used in patients with severe congenital protein C deficiency, antibodies inhibiting protein C may develop.
CEPROTIN is indicated in purpura fulminans andcoumarin-induced skin necrosis in patients with severe congenital protein C deficiency.
Bladder exstrophy is a severe congenital malformation in which the children had bladder no front wall and the corresponding wall of the abdomen.
No formal clinical study in either paediatric orneonatal population with severe congenital protein C deficiency was ever conducted.
In patients, children or adults with severe congenital, cyclic, or idiopathic neutropenia with an absolute neutrophil count(ANC) of≤ 0.5 x 10.
The lack of folic acid in the body of a woman expecting a baby can lead to the birth of a baby with severe congenital pathologies of development.
Filgrastim should not be administered to patients with severe congenital neutropenia(Kostman's syndrome) with abnormal cytogenetics(see below).
Severe congenital cardiac diseases are usually diagnosed in infancy as babies with such anomalies show severe symptoms from birth.
If the preparation is used in patients with severe congenital protein C deficiency, antibodies inhibiting protein C may develop.
Javier, the donor conceived and born after a Preimplantation Genetic Diagnosis(PGD), and his brother Andrés, aged 7,who suffered from an incurable severe congenital anemia.
Successful delivery of patients with severe congenital and acquired heart defects can be facilitated by delivery in hyperbaric oxygenation.
The Committee for Medicinal products for Human Use(CHMP)decided that CEPROTIN' s benefits are greater than its risks for patients with severe congenital protein C deficiency.
Filgrastim should not be administered to patients with severe congenital neutropenia who develop leukaemia or have evidence of leukaemic evolution.
CEPROTIN is used in the treatment and prevention of thrombotic and haemorrhagic skin lesions(named purpura fulminans)in patients with severe congenital protein C deficiency.
Patients who are severely immunocompromised(e.g. patients with severe congenital or acquired cellular and/or humoral immune deficiency)(see section 4.4).
In patients with severe congenital protein C deficiency, CEPROTIN improved all 16 cases of purpura fulminans and all six episodes of coumarin-induced skin necrosis.
Imlygic is not to be used in patients who are severely immunocompromised(e.g. patients with severe congenital or acquired cellular and/or humoral immune deficiency).
Dandy-Walker(DW) malformation is a rare and severe congenital anomaly of the posterior fossa affecting the development of the cerebellum and the fourth ventricle.
Therefore vitamins during pregnancy andpregnancy directly to be taken as 75% of the folic acid prevents severe congenital pathologies of the nervous system of the child.
Children born with Patau Syndrome usually have severe congenital heart defects and other malformations and are unlikely to survive beyond the first year of life.
Furthermore CEPROTIN is used to prevent thrombosis in patients with severe congenital protein C deficiency if one or more of the following conditions are met.
Early births are a risk factor for fetal prematurity, severe congenital disorders, high child mortality during the first year and the health of the mother.