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Holt—Oram综合征,又称家族性心脏上肢异常综合征、心房—手指综合征、上肢心血管综合征。1960年确定为独立疾病。国内报道极少,本院确诊二例,一例合并血小板减少性紫癜,死于心力衰竭,另一例可见隐性脊柱裂。今报告如下: 例一,杨××,男性,2岁10个月,病历号139653。第三胎,第三产,七个月早产,出生体重2400克。生后哭闹时全身发绀,平素易患感冒、
Holt-Oram syndrome, also known as familial heart anorexia syndrome, atrial-finger syndrome, upper extremity cardiovascular syndrome. 1960 was identified as an independent disease. Very few domestic reports, the hospital was diagnosed in two cases, one case complicated with thrombocytopenic purpura, died of heart failure, another case of visible recessive spina bifida. This report is as follows: Example 1, Yang × ×, male, 2 years old 10 months, medical record number 139653. The third child, the third birth, seven months premature birth, birth weight 2400 grams. Whole body cyanosis after birth crying, usually prone to cold,