Wiedemann H R
Eur J Pediatr. 1979 Jan 18;130(1):65-70. doi: 10.1007/BF00441901.
Two male infants with a pseudo-hydrocephalic progeroid syndrome with natal teeth are compared with two very similar female cases reported in the literature and interpreted as congenital progeria. All these cases may represent a separate entity, a previously unrecognized genetic progeroid syndrome.
将两名患有假性脑积水样早老综合征并伴有 natal 牙的男婴与文献中报道的另外两名非常相似的女性病例进行比较，后者被解释为先天性早老症。所有这些病例可能代表一种独立的疾病，即一种此前未被认识的遗传性早老综合征。
