Familial absent pulmonary valve syndrome without deletions of chromosome 22q11
2000 ◽
Vol 10
(6)
◽
pp. 618-620
◽
Keyword(s):
AbstractDeletions of chromosome 22q11 are common in patients with tetralogy of Fallot, and in those with absent pulmonary valve syndrome. In this report, we describe a pair of siblings with absent pulmonary valve syndrome, neither of whom had deletions of chromosome 22q11. The finding of familial absent pulmonary valve syndrome without deletion of 22q11 in our patients suggests an alternative genetic basis for this rare condition.
2011 ◽
Vol 123
(17-18)
◽
pp. 524-525
◽
2006 ◽
Vol 132
(5)
◽
pp. 1099-1104
◽
2008 ◽
Vol 24
(3)
◽
pp. 167-170
1996 ◽
Vol 77
(7)
◽
pp. 547-549
◽
2017 ◽
Vol 27
(9)
◽
pp. 1740-1747
◽
2020 ◽
2015 ◽
Vol 8
(2)
◽
pp. 108
◽