Ferda Percin E, Yilmaz Sarper
Faculty of Medicine, Department of Medical Biology and Genetics, Cumhuriyet University, 58140, Sivas, Turkey.
Clin Dysmorphol. 2003 Oct;12(4):283-4. doi: 10.1097/00019605-200310000-00016.
We report on a case with polydactyly, syndactyly and brachydactyly of the hands and oligodactyly of the feet, but no other anomalies and normal chromosome analysis. We compared the findings in our case with those of brachydactyly B, Fuhrmann syndrome and Haas-type syndactyly. However, it was not possible to suggest a syndrome diagnosis in the present case.
我们报告了一例双手患有多指、并指和短指畸形且双足少指畸形,但无其他异常且染色体分析正常的病例。我们将本病例的发现与短指B型、富尔曼综合征和哈斯型并指畸形的病例进行了比较。然而,在本病例中无法做出综合征诊断。