Warburg M
Hum Hered. 1976;26(2):137-48. doi: 10.1159/000152795.
The heritable falciform folds and congenital retinal non-attachment reported in the literature are here divided into monosymptomatic and complex types. Of the former, autosomal dominant and recessive disorders are known. The complex types comprise several syndromes, both autosomal recessive and X-linked. Retinal dysplasia is sometimes seen in histological sections from these affections, but it is an unspecific histological reaction, and not a disease sui generis. Attention is drawn to the syndrome with microcephaly, microphthalmia and falciform detachment which, though previously described, has not so far been delineated. It is hypothesized that hydrocephaly and congenital retinal non-attachment with or without microphthalmia and persistent hyperplastic primary vitreous constitute yet another 'new' syndrome, mainly seen in females.
文献中报道的遗传性镰状皱襞和先天性视网膜未附着在此分为单症状型和复合型。前者已知有常染色体显性和隐性疾病。复合型包括几种综合征,既有常染色体隐性的,也有X连锁的。在这些病变的组织学切片中有时可见视网膜发育异常,但这是一种非特异性的组织学反应,并非一种独特的疾病。请注意有小头畸形、小眼畸形和镰状脱离的综合征,尽管此前已有描述,但迄今尚未明确界定。据推测,脑积水和伴有或不伴有小眼畸形及永存原始玻璃体增生症的先天性视网膜未附着构成了另一种“新”综合征,主要见于女性。