并指
医学
长QT综合征
内科学
儿科
心脏病学
猝死
QT间期
外科
作者
Melinda L. Marks,Donald L. Trippel,Mark T. Keating
标识
DOI:10.1016/s0002-9149(99)80216-1
摘要
The identification of female children with this syndrome is evidence that this disorder is not X-linked in inheritance. Possible inheritance modes still include autosomal recessive or, more likely, a de novo mutation, given the absence of family history in any of the patients. Children of both sexes with syndactyly should be screened with an electrocardiogram for this syndrome. Female children with this syndrome may have an increased risk of sudden death similar to male children.
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