ATRESIA PULMONAR CIV PDF

As comunicações interventriculares (CIV), na forma isolada, são, de longe, a comunicação interventricular com atresia pulmonar (CIV/AP), a transposição das . La atresia pulmonar es una enfermedad del corazón presente ya en el momento del nacimiento, por lo que se incluye dentro del grupo de enfermedades. Atresia Pulmonar con Septo Interventricular cerrado. Doble Emergencia del pulmonar a la prueba de oxígeno: Cierre de CIV o Si RPT > 7 uds y posible.

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Rosa I ; Paulo Ricardo G.

atresoa To review clinical, etiological and diagnostic characteristics of the 22q11 deletion syndrome and cciv as-sociation with congenital heart defects. Medline, Lilacs and SciELO databases were searched from to using specific descrip-tors as “22q11”, “DiGeorge syndrome”, “velocardiofacial syndrome”, “congenital heart defects” and “cardiovascular malformations”.

Heart malformations are the most fre-quent congenital defects at birth and represent an important Public Health problem. The 22q11 deletion syndrome, also called DiGeorge syndrome, velocardiofacial syndrome and CATCH22, stands out as one of the main known causes of congenital heart defects.

This is an autosomal dominant genetic disease characterized by a highly variable phenotype, which renders its difficult clinical identification. In addition, the pulmonr of the patients present a microdeletion identified mainly by molecular cytogenetic techniques as fluorescent in situ hybridization, which are rarely available in Brazil. Similarly to other syndromes, 22q11 deletion syndrome is associated to some specific heart defects, espe-cially conotruncal.

It is still not clear which patients with congenital heart defect should be screened for 22q11 dele-tion syndrome. Cardiologists and cardiac surgeons, particu-larly the pediatric ones, must be aware about the features and health care related to 22q11 deletion syndrome.

Subjects with the syndrome very often present abnormalities of mul-tiple systems, that cic result in difficulties and complica-tions during their clinical and surgical course.

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ateesia Rev Paul Pediatr ; Rev Assoc Med Bras ; Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q Mol Cell Biochem ; Recognizing a common genetic syndrome: PCR screening for 22q Clin Chim Acta ; A population study of chromosome 22q11 deletions in infancy.

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Atresia pulmonar | American Heart Association

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Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and pumlonar arch: A genetic etiology for interruption of the aortic arch type B. Am J Cardiol ; Frequency of 22q11 deletions in patients with conotruncal defects.

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Atresia pulmonar – Wikipedia, la enciclopedia libre

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Atresia pulmonar

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