LR99ES10 Laboratory of Human genetics, Faculty of Medicine of Tunis, University of Tunis El Manar, Tunis, Tunisia.
Fetopathology Unit, Hospital Habib Bougatfa, Bizerte, Tunisia.
Fetal Pediatr Pathol. 2022 Apr;41(2):179-197. doi: 10.1080/15513815.2020.1775735. Epub 2020 Jun 18.
The aim of this study was to classify the fetal skeletal dysplasias (FSD) in a series of affected fetuses based on radio-pathologic criteria. We gathered clinicopathologic data of 72 cases which were diagnosed among 5995 autopsies performed over a 8-year period. The prevalence of FSD was 1.2:100 autopsies. The overall sex ratio (M:F) was 1.25. Gestational age was between 17 and 24 weeks in 60% of cases. The FSD were classified into 13 distinct pathologic groups. Four major groups were identified: (1) Osteogenesis imperfecta (21 cases, 29%); (2) chondrodysplasia (18 cases, 25%); (3) Ciliopathies (9 cases, 12%); and (4) Sulfation disorders (7 cases, 10%). Thanatophoric dysplasia type 1 and lethal osteogenesis imperfecta were the most common skeletal dysplasias. Our study demonstrates the usefulness of the radio-pathologic examination in the diagnosis and accurate classification of the FSD, thus enabling better targeting of genetic counseling.
本研究旨在根据放射病理学标准对一系列受影响胎儿中的胎儿骨骼发育不良(FSD)进行分类。我们收集了在 8 年期间进行的 5995 例尸检中诊断出的 72 例病例的临床病理数据。FSD 的患病率为 1.2:100 例尸检。总体性别比例(M:F)为 1.25。60%的病例中,胎龄在 17 至 24 周之间。FSD 分为 13 个不同的病理组。确定了四个主要组:(1)成骨不全症(21 例,29%);(2)软骨发育不良(18 例,25%);(3)纤毛病(9 例,12%);和(4)硫酸盐代谢障碍(7 例,10%)。Thanatophoric 发育不良 1 型和致死性成骨不全症是最常见的骨骼发育不良。我们的研究表明,放射病理学检查在 FSD 的诊断和准确分类中非常有用,从而能够更好地进行遗传咨询。