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  2. 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.

  3. 2022 Central Visual and Performing Arts High School shooting

    en.wikipedia.org/wiki/2022_Central_Visual_and...

    The school also has several metal detectors, and seven security guards were present on the day of the shooting. [3] [5] Missouri does not have a red flag law which permits a state court to order the temporary removal of firearms from a person who they believe may present a danger to others or themselves. [6] [7]

  4. Persistent truncus arteriosus - Wikipedia

    en.wikipedia.org/wiki/Persistent_Truncus_Arteriosus

    Persistent truncus arteriosus (PTA), [1] often referred to simply as truncus arteriosus, [2] is a rare form of congenital heart disease that presents at birth. In this condition, the embryological structure known as the truncus arteriosus fails to properly divide into the pulmonary trunk and aorta .

  5. 12-year-old joins Marines for boot camp at Parris Island. ‘He ...

    www.aol.com/12-old-joins-marines-boot-172148810.html

    Trent Williams, who has a congenital heart defect, could have gone anywhere but his wish was to experience the military’s toughest boot camp 12-year-old joins Marines for boot camp at Parris Island.

  6. Interrupted aortic arch - Wikipedia

    en.wikipedia.org/wiki/Interrupted_aortic_arch

    Interrupted aortic arch is a very rare heart defect (affecting 3 per million live births) [1] in which the aorta is not completely developed. There is a gap between the ascending and descending thoracic aorta. In a sense it is the complete form of a coarctation of the aorta. Almost all patients also have other cardiac anomalies, including a ...

  7. 1q21.1 duplication syndrome - Wikipedia

    en.wikipedia.org/wiki/1q21.1_duplication_syndrome

    1q21.1 duplication syndrome, also known as 1q21.1 microduplication, is an uncommon copy number variant associated with several congenital abnormalities, including developmental delay, dysmorphic traits, autism spectrum disorder, and congenital cardiac defects. [1] Common facial features include frontal bossing, hypertelorism, and macrocephaly.

  8. Ebstein's anomaly - Wikipedia

    en.wikipedia.org/wiki/Ebstein's_anomaly

    Ebstein's anomaly is a congenital heart defect in which the septal and posterior leaflets of the tricuspid valve are displaced downwards towards the apex of the right ventricle of the heart. [1] EA has great anatomical heterogeneity that generates a wide spectrum of clinical features at presentation and is complicated by the fact that the ...

  9. Atrial septostomy - Wikipedia

    en.wikipedia.org/wiki/Atrial_septostomy

    Atrial septostomy is a surgical procedure in which a small hole is created between the upper two chambers of the heart, the atria.This procedure is primarily used to palliate dextro-Transposition of the great arteries or d-TGA (often imprecisely called transposition of the great arteries), a life-threatening cyanotic congenital heart defect seen in infants.