copy and paste this google map to your website or blog!
Press copy button and paste into your blog or website.
(Please switch to 'HTML' mode when posting into your blog. Examples: WordPress Example, Blogger Example)
Input Form:Deal with this potential dealer,buyer,seller,supplier,manufacturer,exporter,importer
(Any information to deal,buy, sell, quote for products or service)
Congenital pulmonary airway malformation - UpToDate Congenital pulmonary airway malformation (CPAM), previously known as congenital cystic adenomatoid malformation (CCAM), is a rare developmental anomaly of the lower respiratory tract [1,2]
Congenital pulmonary airway malformation - Wikipedia Congenital pulmonary airway malformation (CPAM), formerly known as congenital cystic adenomatoid malformation (CCAM), is a congenital disorder of the lung similar to bronchopulmonary sequestration
Congenital Cystic Pulmonary Malformation (CPAM or CCAM) CPAM is sometimes referred to as congenital cystic adenomatoid malformation (CCAM) How is CPAM diagnosed? With improvement in prenatal imaging technology, most CPAMs are detected during a routine prenatal ultrasound A fetal MRI or fetal echocardiogram may also be used to confirm the diagnosis
Fetal Congenital Cystic Adenomatoid Malformation (CCAM) A CCAM is a benign mass of abnormal lung tissue that replaces part of one lobe of a fetal lung CCAMs can occur in either lung and are classified into three different types based on the size of the cyst or cysts
Congenital Pulmonary Airways Malformation (CPAM) A congenital pulmonary airway malformation (CPAM), also known as congenital cystic adenomatoid malformation (CCAM), is a cystic piece of abnormal lung tissue that does not work like normal lung tissue
Congenital Cystic Adenomatoid Malformation (CCAM) Congenital cystic adenomatoid malformation (CCAM), also known as congenital pulmonary airway malformation (CPAM), is an abnormal growth of lung tissue arising from various parts of the airway that can compress normal lung tissue and affect lung development