oligohydramnios/proline

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Cloacal dysgenesis sequence: observations in four patients including three fetuses of second trimester gestation.

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Cloacal dysgenesis is a rare malformation sequence. We studied cloacal dysgenesis in four fetuses, including three at 18-22 weeks of gestation. All four fetuses showed a smooth perineum with absence of anal, urethral, and/or vaginal openings. The urinary bladder was dilated in 3 cases. The labia

The lungs in congenital bilateral renal agenesis and dysplasia.

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A detailed quantitative analysis was made of the lungs from 8 infants dying with bilateral renal agenesis or dysplasia. Total lung volume was reduced in all cases, particularly in those with renal agenesis. In both groups there was a reduction in number of airway generations, indicating interference

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Herbal & Natural Medicine

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