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Among children with one kidney, there are approximately twice as many males, whereas among children with three kidneys there are approximately 2.5 times more females. The same pattern is observed among infants with excessive number of ribs, vertebrae, teeth and other organs which in a process of evolution have undergone reduction—among them ...
Fetal warfarin syndrome is a disorder of the embryo which occurs in a child whose mother took the medication warfarin (brand name: Coumadin) during pregnancy.Resulting abnormalities include low birth weight, slower growth, intellectual disability, deafness, small head size, and malformed bones, cartilage, and joints.
Signs and symptoms of preterm labor include four or more uterine contractions in one hour. In contrast to false labour, true labor is accompanied by cervical dilation and effacement. Also, vaginal bleeding in the third trimester, heavy pressure in the pelvis, or abdominal or back pain could be indicators that a preterm birth is about to occur.
Disability-adjusted life year for childhood-cluster diseases per 100,000 inhabitants. These include pertussis , poliomyelitis , diphtheria , measles , and tetanus . no data
Placental abruption defined as the separation of the placenta from the uterus prior to delivery, is a major cause of third trimester vaginal bleeding and complicates about 1% of pregnancies. [13] [50] Symptomatic presentations are variable: Some women can entirely ignore the symptoms, while others have mild bleeding or abdominal discomfort and ...
If the infection occurs 12–20 weeks after conception, the risk is 20%. Infants are not generally affected if rubella is contracted during the third trimester. [3] Diagnosis of congenital rubella syndrome is made through a series of clinical and laboratory findings and management is based on the infant's clinical presentation.
List of ICD-9 codes 740–759: congenital anomalies; Rare disease This page was last edited on 28 September 2024, at 13:01 (UTC). Text is available under the Creative ...
Cystic hygromas that develop in the third trimester, after 30 weeks' gestation, or in the postnatal period are usually not associated with chromosome abnormalities. A chance exists of recurrence after surgical removal of the cystic hygroma. The chance depends on the extent of the cystic hygroma and whether its wall was completely removed. [10]