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Pulmonary agenesis is an inborn lung underdevelopment that is rare and potentially lethal. [1] The disorder is caused by a complete developmental arrest of the primitive lung during embryonic life, and it is often associated with other developmental defects. [2]
Congenital pulmonary airway malformation in a fetus, ultrasound at 19 weeks - transverse. Stomach on left image; heart on right image: displaced to right by cystic mass. The earliest point at which a CPAM can be detected is by prenatal ultrasound. The classic description is of an echogenic lung mass that gradually disappears over subsequent ...
752 Congenital anomalies of genital organs. 752.0 Congenital anomalies of ovaries; 752.1 Congenital anomalies of fallopian tubes and broad ligaments; 752.2 Doubling of uterus; 752.3 Other congenital anomalies of uterus; 752.4 Anomalies of cervix, vagina, and external female genitalia. 752.42 Imperforate hymen; 752.43 Cervical agenesis; 752.5 ...
Pulmonary artery agenesis refers to a rare congenital absence of pulmonary artery due to a malformation in the sixth aortic arch. It can occur bilaterally, with both left and right pulmonary arteries being absent, or unilaterally, the absence of either left or right pulmonary artery (UAPA).
Incidence of congenital malformations associated with tracheal agenesis. Results were obtained from a total of 32 individual case studies. [11]The classic in-utero symptoms of tracheal agenesis are an absence of the trachea leading to congenital high airway obstruction syndrome, [12] [13] lung distention, polyhydramnios, heart malformations, heart displacement and hydrops fetalis.
Medical diagnosis of pulmonary hypoplasia in utero may use imaging, usually ultrasound or MRI. [12] [13] The extent of hypoplasia is a very important prognostic factor. [14]One study of 147 fetuses (49 normal, 98 with abnormalities) found that a simple measurement, the ratio of chest length to trunk length, was a useful predictor of postnatal respiratory distress. [15]
This is the most common surgery done to correct dextro-TGA, and is considered the definitive treatment. The atrial switch operation is an alternative surgical option when the arterial switch is not feasible due to the particular coronary artery anatomy. This operation creates a tunnel (baffle) between the heart's two upper chambers (atria). [2]
Embryologically, it arises from an anomalous lateral course of the azygos vein, [3] in a pleural septum within the apical segment of the right upper lobe or in other words an azygos lobe is formed when the right posterior cardinal vein, one of the precursors of the azygos vein, fails to migrate over the apex of the lung and penetrates it ...