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方可尼氏贫血(Fanconi’s Anemeia)是一种先天性、家族性再生障碍性贫血,又名先天性全血细胞减少症,常伴多发性先天性畸形,该病为常染色体隐性遗传病,最近有人将此病归入DNA修复病(Diseases of DNA Repair)。据国外统计已有200多例报导,发病率为1/70,000—1/360,000。国内也有个别报导,现将我科在1981年5月收治的一例报告如下: 患儿,男性,12,四岁起经常鼻衄;8—9岁起经常牙龈出血,近5个月来出现头昏,进行性苍白,下肢紫癜而入院,在外曾诊断
Fanconi’s Anemeia is a congenital, familial aplastic anemia, also known as congenital pancytopenia, often accompanied by multiple congenital malformations, the disease is autosomal recessive disease, the recent Someone put the disease into DNA repair disease (Diseases of DNA Repair). According to statistics from abroad, there are more than 200 cases reported, the incidence rate of 1 / 70,000-1 / 360,000. There are also individual reports in our country. The report of one case admitted to our department in May 1981 is as follows: Children, males, 12 or 4 years old often have epistaxis; bleeding gums often occur in 8-9 years old and head in the past 5 months Faint, progressive pale, purpura and lower extremity admission, had been diagnosed