DNA-based prenatal exclusion of bullous congenital ichthyosiform erythroderma at the early stage, 10 to 11 weeks' of pregnancy, in two consequent siblings - 24/08/11
Doi : 10.1016/j.jaad.2004.06.020
Yukiko Tsuji-Abe, MD a, Masashi Akiyama, MD, PhD a, ⁎ 
, Hideki Nakamura a, Yasuko Takizawa, DVM, PhD b, Daisuke Sawamura, MD, PhD a, Kayoko Matsunaga, MD, PhD c, Kaoru Suzumori, MD, PhD d, Hiroshi Shimizu, MD, PhD a
, Hideki Nakamura a, Yasuko Takizawa, DVM, PhD b, Daisuke Sawamura, MD, PhD a, Kayoko Matsunaga, MD, PhD c, Kaoru Suzumori, MD, PhD d, Hiroshi Shimizu, MD, PhD a a From the Departments of Dermatology at Hokkaido University Graduate School of Medicine, Sapporo
b Keio University School of Medicine, Tokyo
c Fujita Health University School of Medicine, Toyoake
d Department of Obstetrics and Gynecology, Nagoya City University School of Medicine
Reprint requests: Masashi Akiyama, MD, PhD, Department of Dermatology, Hokkaido University Graduate School of Medicine, North 15, West 7, Kita-ku, Sapporo 060-8638, Japan.Sapporo, Tokyo, Toyoake, and Nagoya, Japan
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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| Supported in part by a Grant-in-Aid from the Ministry of Education, Science, Sports, and Culture of Japan (No. 16390312 to M. Akiyama). Conflicts of interest: None identified. |
© 2004
American Academy of Dermatology, Inc.. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 51 - N° 6
P. 1008-1011 - décembre 2004 Retour au numéro
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