Erondu–Cymet Syndrome
Chromosome 21 (human), Karyotype, Tyler Cymet, Down syndrome, Human Genome Project
978-620-0-83887-2
6200838879
52
2012-03-06
29.00 €
eng
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Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Erondu–Cymet syndrome is a syndrome caused by a translocation on the . The genetic for people with this condition is 46, XY, inv(21)(q11.2q22.1). Findings in these patients include: hypotension, hypoxemia, seizures, and impairment of cognitive ability. Patients with this condition may have persistent left superior vena cava that drains into the left atrium, as well as pulmonary arterio-venous malformations. Erondu–Cymet Syndrome was discovered in 2006 by Ugochi Erondu and . In 2000, researchers working on the announced that they had determined the sequence of that make up this chromosome. Chromosome 21 was the second human chromosome to be fully sequenced.
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