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Congenital pulmonary airway malformation (CPAM), formerly known as congenital cystic adenomatoid malformation (CCAM), is a congenital disorder of the lung similar to bronchopulmonary sequestration. In CPAM, usually an entire lobe of lung is replaced by a non-working cystic piece of abnormal lung tissue.
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Congenital cystic adenomatoid malformation, now known as congenital pulmonary airway malformation (CPAM) cCam, a camera capture program that runs on Nokia S60 phones; Center for research on Children, Adolescents, and the Media at the University of Amsterdam, the Netherlands
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Causes of pulmonary hypoplasia include a wide variety of congenital malformations and other conditions in which pulmonary hypoplasia is a complication. [1] These include congenital diaphragmatic hernia, congenital cystic adenomatoid malformation, fetal hydronephrosis, caudal regression syndrome, mediastinal tumor, and sacrococcygeal teratoma with a large component inside the fetus.
Congenital adrenal hyperplasia (CAH) Congenital central hypoventilation syndrome; Congenital diaphragmatic hernia (CDH) Congenital Disorder of Glycosylation (CDG) Congenital hyperinsulinism; Congenital insensitivity to pain with anhidrosis (CIPA) Congenital pulmonary airway malformation (CPAM) Conjoined twins; Costello syndrome; Craniopagus ...
747.3 Congenital anomalies of pulmonary artery; 747.4 Congenital anomalies of great veins; 747.5 Absence or hypoplasia of umbilical artery; 747.6 Arteriovenous malformation, unspec. 747.8 Other specified anomalies of circulatory system. 747.81 Congenital anomalies of cerebrovascular system; 747.82 Spinal vessel anomaly; 747.83 Persistent fetal ...