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Maternal risks and predictor factors for the termination of pregnancy in fetuses with severe congenital anomaly: experience from a single reference center in brazil
(Wiley, 2016)
Objective: To assess the maternal complications in pregnant women with fetuses with several congenital anomaly as well as the predictor variables for the termination of pregnancy.Methods: We performed a retrospective cohort ...
Severe visual impairment and blindness in infants: causes and opportunities for control
(Medknow Publications, 2014)
A new surgical technique for congenital distichiasis
(2018-03-04)
Purpose: To describe a new technique to treat congenital distichiasis. Methods: Case series of three distichiatic patients undergoing a novel surgical technique combining splitting of the lid margin with the distichiatic ...
Congenital temporomandibular joint ankylosis: Clinical characterization and natural history of four unrelated affected individuals
(Alliance Communications Group Division Allen PressLawrenceEUA, 2005)
Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies
(2015-12-01)
Terminal deletion in the short arm of chromosome 1 results in a disorder described as 1p36 deletion syndrome. The resulting phenotype varies among patients including mental retardation, developmental delay, sensorineural ...
Prenatal detection of congenital anomalies and related factors in Argentina
(Springer, 2020-07)
Congenital anomalies (CAs) are a leading cause of neonatal death. Many CAs can be diagnosed prenatally. To estimate the prenatal detection rate (PDR) of CA in hospitals participating in the RENAC (National Network of ...
Very rare defects: what can we learn?
(Wiley, 2017)