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Issue Information

Author(s) -

Keiko Shimojima,

Nobuhiko Okamoto,

Toshiyuki Yamamoto,

Akane Kitamura,

Naoko Miyauchi,

Hirotaka Hamada,

Hitoshi Hiura,

Hatsune Chiba,

Hiroaki Okae,

Akiko Satô,

Rosalind M. John,

Takahiro Arima,

Stelios Mavrogenis,

Nándor Ács,

Andrew E. Czeizel,

Zhi-cai Shi,

Quan Li,

Bin Cai,

Baoqing Yu,

Yuan Feng,

Jibin Wu,

Ming Li,

Bo Ran,

Toshio Okamoto,

Ken Nagaya,

Yumi Kawata,

Hiroko Asai,

Etsushi Tsuchida,

Fumikatsu Nohara,

Kazuki Okajima,

Hiroshi Azuma,

Giovanna Cantarella,

Michele Gaffuri,

Lorenza Pugni,

Lorenzo Pignataro,

Fabio Prenatal,

Yuko Hayashi,

Nobuhiro Suzumori,

Tokio Sugiura,

Mayumi SugiuraOgasawara,

Ryo Kiyokoba,

Nobuhiro Hidaka,

Yukiyo Sakata,

Kazuhisa Hachisuga,

Kotaro Fukushima,

Kiyoko Kato,

Toshiki Takenouchi,

Midori Awazu,

Thomas Eggermann,

Kenjiro Kosaki,

Özlem Boybeyi,

İsmail Özmen,

Yasemin Dere Günal,

Mustafa Kemal Aslan,

Didem Aliefendioğlu,

Alessia Coralli,

Yuji Nakajima,

Hiroaki Aoyama,

Joso Hatta,

Kenji Uchinada,

Yokohama Kurosawa,

Toshiyuki Managing Editor,

Osaka Yamagishi,

Nigel Brown,

Chiristina Chambers,

San Diego,

Robert E. Chapin,

Makoto Ema,

John D. Graham,

Angeles Hirahara,

Y. S. Lewis,

B Holmes,

Sachiko Iseki,

Han-Sung Jung,

Susan L. Makris,

Masashi Mizuguchi,

Tokyo Muenke,

Tetsuji Bethesda,

Higashiosaka Nagao,

Ichiro Gifu,

Yonago Naruse,

Toshihiko Tokyo,

Y. Ogino,

Osaka Okamoto,

Izumo Otani,

Elisabeth Padmanabhan,

Kohei Lyon,

Shinichi Shiota,

Nagoya Sonta,

G. F. Donald,

Ashland Stump,

Jun Takano,

Otsu Udagawa,

Gen Watanabe,

Wakayama Yamada,

Masako Yamada,

Toshiyuki Sagamihara,

Michiko Yamamoto,

Atsushi Tokyo,

Hiroki Otani

Publication year - 2015

Publication title -

congenital anomalies

Language(s) - English

Resource type - Reports

eISSN - 1741-4520

pISSN - 0914-3505

DOI - 10.1111/cga.12084

Subject(s) - polydactyly , medicine , macrocephaly , hypoplasia , anatomy , pediatrics

Fetal computed tomography (left panel) and postmortem radiography (right panel) of a patient with severe short‐rib polydactyly syndrome type III phenotype show the extremely narrow thorax, the severely shortened tubular bones with round metaphyseal ends and lateral spikes, macrocephaly, high clavicles, polydactyly in both the hands and feet, and hypoplasia of the iliac bones. Further details can be seen in the article by Okamoto et al. in this issue.

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