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Introduction and aims of the study: 1p36 deletion syndrome is the most common terminal deletion in humans, occurring in 1:5000 births, predominantly on females. Most cases are sporadic; a minority is associated with chromosomal duplication. Clinical features include craniofacial dysmorphisms, hypotonia, development delay, epilepsy, hearing loss and also cardiac, cerebral, visual, skeletal and urogenital anomalies.
Introduction and aims of the study: Acute pulmonary edema is a rare complication in pregnancy and postpartum, with an estimated incidence between 0.08 and 0.5%. Acute pulmonary edema is the main cardiovascular complication of preeclampsia and one of the criteria of severe preeclampsia; occurs in 3% of preeclampsia cases, 70% of which take place during postpartum. The main risk factors for acute pulmonary edema in preeclampsia are advanced maternal age, multiparity and chronic hypertension.
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