نتایج جستجو برای: congenital defect
تعداد نتایج: 207564 فیلتر نتایج به سال:
A 6600 g male infant, delivered vaginally at 38 weeks of gestation with a birth weight of 3500 g, was found to have moderate hepatomegaly, mild ascites, lower limbs edema, oliguria, hyponatremia, leukocytosis (24.8 10 cellsmm ) and severe anemia (5 g dl ) without apparent cause at 2 months and 17 days after birth. The mother had no antenatal care but at birth he was apparently healthy until day...
BACKGROUND Several genetic defects are associated with permanent congenital hypothyroidism. Immunologic, environmental, and iatrogenic (but not genetic) factors are known to induce transient congenital hypothyroidism, which spontaneously resolves within the first months of life. We hypothesized that molecular defects in the thyroid oxidase system, which is composed of at least two proteins, mig...
This is the case of a male newborn whose mother during pregnancy was treated with chloropromazine, topiramate and diazepam, but without any other relevant family history, especially related with congenital malformation. At 34 weeks of gestation, the fetus was diagnosed with transposition of the great arteries (TGA). He born at 37 weeks of gestation, his birth weight was 3,229g and Apgar score 1...
A 68-year-old female with no significant past medical history presented with loss of vision in the lower half of her left eye that lasted <5 minutes. No abnormalities were found on ocular or physical exam. Computed tomography angiography and carotid ultrasound were performed, which confirmed the diagnosis as amaurosis fugax with two abnormalities leading to the transient retinal vessel occlusio...
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