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Ruzicka Goerz Anton syndrome : ウィキペディア英語版 | Ruzicka Goerz Anton syndrome
Ruzicka Goerz Anton syndrome is a rare genetic disease described by Ruzicka et al. in 1981. It is characterized by icthyosis (rough, scaly skin), deafness, intellectual disability, and skeletal anomalies.〔(【引用サイトリンク】 publisher=Check Orphan )〕 It is also known as "Ichthyosis deafness intellectual disability skeletal anomalies". ==Symptoms== The primary symptoms of Ruzicka Goerz Anton syndrome include ichthyosis, deafness, oligophrenia, and skeletal deformities.〔
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Ruzicka Goerz Anton syndrome」の詳細全文を読む
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