Erondu–Cymet syndrome

From WikiProjectMed
Jump to navigation Jump to search

Erondu–Cymet syndrome is a syndrome caused by a translocation on the 21st chromosome.[1] The genetic karyotype 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.[1] Patients with this condition may have persistent left superior vena cava that drains into the left atrium, as well as pulmonary arteriovenous malformations. Erondu–Cymet syndrome was discovered in 2006 by Ugochi Erondu and Tyler Cymet.[1]

See also

References

  1. ^ a b c Erondu, U. A.; Cymet, T. C. (Winter 2006). "Chromosome 21 abnormalities a review and report of a case of erondu-cymet syndrome". Comprehensive Therapy. 32 (4): 254–260. doi:10.1007/BF02698072. PMID 17898432. S2CID 37968241.


Stub icon

This genetic disorder article is a stub. You can help Wikipedia by expanding it.

Retrieved from "https://mdwiki.org/wiki/Erondu–Cymet_syndrome"