Czeizel A E, Vitéz M, Kodaj I, Lenz W
Department of Human Genetics and Teratology, National Institute of Hygiene, WHO Collaborating Centre for the Community Control of Hereditary Diseases, Budapest, Hungary.
Acta Morphol Hung. 1992;40(1-4):71-86.
A population-based and validated data set of 14 cases with isolated proximal intercalary type of congenital limb deficiency born in Hungary between 1975-84 was evaluated. Two cases had phocomelia of upper limbs, while 12 cases were affected with classical intercalary defects mainly in femurs. Of 14 cases, 13 had unimelic manifestation and both sexes were equally affected. The intrauterine growth retardation, the excess of second birth order, a higher rate of acute maternal disorder of the respiratory system and the lack of familial cluster are noteworthy. The vascular disruption hypothesis seems to be the most plausible explanation for the origin of isolated proximal intercalary defects.
对1975年至1984年间出生在匈牙利的14例孤立性近端节间型先天性肢体缺损病例的基于人群且经过验证的数据集进行了评估。2例有上肢短肢畸形,而12例主要是股骨出现典型的节间缺损。在14例病例中,13例有单肢表现,男女受影响程度相同。宫内生长迟缓、二胎出生率过高、急性母体呼吸系统疾病发生率较高以及缺乏家族聚集性值得注意。血管破坏假说似乎是孤立性近端节间缺损起源的最合理的解释。