polyhydramnios/albumin

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Biochemical composition of fluids for amnioinfusion during fetoscopy.

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OBJECTIVE To evaluate which of the commercially available solutions is best suited for amnioinfusion during fetoscopy, based on resemblance with the biochemical properties of amniotic fluid. METHODS Amniotic fluid samples from 10 pregnancies were studied. Specimens were obtained from 5 pathologic

Pregnancy in a patient with congenital analbuminaemia.

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Congenital analbuminaemia is a rare autosomal recessive disorder that is characterised by a severe reduction or total absence of serum albumin. This condition has implications for therapeutics as a large proportion of commonly used drugs are plasma protein bound where albumin is the primary

[Medical treatment of chylous effusions in newborn infants. Apropos of 3 cases].

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BACKGROUND Chylous effusions are the most frequent cause of non immunologic hydrops fetalis. They can be recognized antenatally by ultrasonography. Their evacuation is sometimes necessary and medical treatment often effective. METHODS Case n. 1: fetal ascites was detected by ultrasonography at the

Association of Bartter's syndrome and empty sella.

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Bartter's syndrome is characterized by hypochloremia, hypokalemia, metabolic alkalosis associated with renal potassium leakage, and normal blood pressure despite increased plasma renin activity. Although association of empty sella with Gitelman syndrome has been reported, no association has been

Radiology of non-immune hydrops fetalis.

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A woman presented with polyhydramnios when 33 weeks pregnant, and three weeks later delivered an infant with idiopathic non-immune hydrops fetalis. Ultrasonic scanning before birth showed a severely edematous infant. An abdominal radiograph revealed the classical "Buddha" position of fetal hydrops.

[A pregnant patient with anti-MuSK antibody positive myasthenia gravis and her infant with transient neonatal myasthenia gravis].

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A 30-year-old healthy woman experienced speech disturbance and swallowing difficulty at two months of pregnancy. She was diagnosed as myasthenia gravis (MG) with anti-MuSK antibodies. At eight months of pregnancy, bulbar palsy, eye movement disturbance, and muscle weakness worsened unexpectedly.

[Intrauterine fetal therapy of NIHF with massive pleural effusion - a case study].

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Hydrops fetalis (fetal hydrops) is a serious fetal condition defined as abnormal accumulation of fluid in two or more extravascular compartments, including ascites, pleural effusion, pericardial effusion, and skin edema. Edema is classified as immune or non-immune. Today more than 90% of fetal edema

A case of fetal intestinal tract distensions: prenatal biochemical and ultrasound evaluation.

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Fetal intestinal tract abnormalities can be pregnancy complications at all maternal ages. There have been reports of ultrasound identification of these abnormalities, particularly of fetal intestinal obstructions. We report the first case to our knowledge of elevated levels of the intestinal

What about the renal function during childhood of children born from dialysed mothers?

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BACKGROUND Pregnancy during dialysis is a high-risk condition which is becoming more and more common. The renal outcome of children born from such pregnancies needs to be investigated since renal development may be affected (i.e. exposure to uraemic toxins, therapies, intermittent haemodynamic

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