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早老综合征(Progeria syndrome)最早由Hutchinson(1886)和Gilford(1904)报道,故又称Hutchinson-Gilford综合征。本病以侏儒、早老、早卒为特征,可能是胶原异常所致。DeBusk(1972)已总结过60例,国内报道较少。患儿常×男11岁湖南衡阳人双眼视物不清11年,流泪2年,起白膜2个月。患儿为三孕二胎,足月顺产,出生体重2.3kg。母孕期2个月时有先兆流产征。父母非近亲婚配,家族无类似患者。营养发育差,体重13kg,身高100cm,
Progeria syndrome was first reported by Hutchinson (1886) and Gilford (1904), so it is also called Hutchinson-Gilford syndrome. The disease is characterized by dwarfism, premature old age, premature death, may be caused by collagen abnormalities. DeBusk (1972) has concluded 60 cases, less reported in the country. Children often × male and 11-year-old Hengyang, Hunan binocular vision is unclear 11 years, tears 2 years, from the white film 2 months. Children with third trimester second child, full-term natural delivery, birth weight 2.3kg. Pregnancy 2 months when threatened abortion sign. Parents are married to non-relatives and have no similar family. Poor nutrition, weight 13kg, height 100cm,