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  2. Congenital heart defect - Wikipedia

    en.wikipedia.org/wiki/Congenital_heart_defect

    Contents. Congenital heart defect. A congenital heart defect (CHD), also known as a congenital heart anomaly, congenital cardiovascular malformation, and congenital heart disease, is a defect in the structure of the heart or great vessels that is present at birth. [ 7 ] A congenital heart defect is classed as a cardiovascular disease. [ 10 ]

  3. CDK13-related disorder - Wikipedia

    en.wikipedia.org/wiki/CDK13-related_disorder

    CDK13-related disorder, also known as congenital heart defects, dysmorphic facial features and intellectual developmental disorder (CHDFIDD), is a very rare autosomal dominant genetic condition characterised by congenital heart defects, intellectual disability and characteristic facial features. Those affected typically have motor and language ...

  4. Children's Heart Foundation hosts Congenital Heart Walk to ...

    www.aol.com/news/childrens-heart-foundation...

    The Children's Heart Foundation is hosting one of its 33 heart walks in Gilbert to raise awareness for what the CDC says is the most common type of defects in newborns.

  5. Eisenmenger syndrome - Wikipedia

    en.wikipedia.org/wiki/Eisenmenger_syndrome

    Eisenmenger syndrome or Eisenmenger's syndrome is defined as the process in which a long-standing left-to-right cardiac shunt caused by a congenital heart defect (typically by a ventricular septal defect, atrial septal defect, or less commonly, patent ductus arteriosus) causes pulmonary hypertension [1] [2] and eventual reversal of the shunt into a cyanotic right-to-left shunt.

  6. Overcoming congenital defect, WSU student puts heartfelt ...

    www.aol.com/overcoming-congenital-defect-wsu...

    A Washington State University sophomore on the school's cheer team, Reyes, 19, knows what it's like to have heart issues as a survivor of a congenital heart defect called Tetralogy of Fallot.

  7. DiGeorge syndrome - Wikipedia

    en.wikipedia.org/wiki/DiGeorge_syndrome

    Depends on the specific symptoms [3] Frequency. 1 in 4,000 [7] DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by a microdeletion on the long arm of chromosome 22. [7] While the symptoms can vary, they often include congenital heart problems, specific facial features, frequent infections, developmental ...

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