论文部分内容阅读
先天性甲状腺缺如症是一种常染色体隐性遗传病,临床少见,多为散在发生,笔者遇一家之中姐弟5人均患此病,现报告如下: 例1,男孩,为第1胎足月顺产,出生体重4kg,母乳喂养。出生后第8天其母发现比出生时明显消瘦,呈进行性萎缩,最后体重减至0.6kg,呈衰竭状态,存活80天死亡。 例2,女孩,为第2胎足月顺产,出生体重3kg。发病过程与例1相同,存活99天死亡。
Congenital hypothyroidism is an autosomal recessive disease, clinical rare, mostly scattered occurrence, I met one of the siblings 5 were suffering from the disease, are reported as follows: Example 1, the first child Full-term birth, birth weight 4kg, breastfeeding. On the 8th day after birth, her mother found that her mother was significantly wasting more than she was born and showed progressive atrophy. At last her weight was reduced to 0.6kg and was in a state of exhaustion, leaving her to die for 80 days. Example 2, girls, full-term birth of the second child birth, birth weight 3kg. The course of disease and the same as in Example 1, the survival of 99 days of death.