DNA-based prenatal exclusion of bullous congenital ichthyosiform erythroderma at the early stage, 10 to 11 weeks' of pregnancy, in two consequent siblings |
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Authors: | Tsuji-Abe Yukiko Akiyama Masashi Nakamura Hideki Takizawa Yasuko Sawamura Daisuke Matsunaga Kayoko Suzumori Kaoru Shimizu Hiroshi |
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Affiliation: | aFrom the Departments of Dermatology at Hokkaido University Graduate School of Medicine, Sapporo;bKeio University School of Medicine, Tokyo;cFujita Health University School of Medicine, Toyoake;dDepartment of Obstetrics and Gynecology, Nagoya City University School of Medicine |
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Abstract: | The proband was a Japanese woman with bullous congenital ichthyosiform erythroderma harboring a keratin 10 gene mutation M150T. DNA-based prenatal exclusion of bullous congenital ichthyosiform erythroderma was successfully performed in her two consequent pregnancies using chorionic villus samples at 10 to 11 weeks' gestation, several weeks earlier than the previously reported cases. |
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