Vasomotor instability in neonates with chromosome 22q11 deletion syndrome

Approximately 70% of individuals with chromosome 22q11 deletion syndrome (22q11DS) have congenital heart defects. A host of other vascular problems in these patients, such as tortuous carotid arteries, Raynaud's phenomenon, unexplained hypotension, hypertension, and hypothermia, raise the possi...

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Veröffentlicht in:	American journal of medical genetics 2003-09, Vol.121A (3), p.231-234
Hauptverfasser:	Shashi, Vandana, Berry, Margaret N., Hines, Michael H.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Arterial hypertension. Arterial hypotension autonomic nervous system Biological and medical sciences Blood and lymphatic vessels Cardiology. Vascular system chromosome 22q11 deletion syndrome Chromosomes, Human, Pair 22 - genetics Clinical manifestations. Epidemiology. Investigative techniques. Etiology congenital heart defects DiGeorge syndrome DiGeorge Syndrome - diagnosis DiGeorge Syndrome - genetics Fatal Outcome Female Gene Deletion Heart Defects, Congenital - genetics Humans Hypotension - genetics Infant, Newborn Male Medical sciences Phenotype Syndrome Vasomotor System - abnormalities Velocardiofacial syndrome Velopharyngeal Insufficiency - diagnosis Velopharyngeal Insufficiency - genetics
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