Thoracomelic dysplasia

Thoracomelic dysplasia is an extremely rare primary bone dysplasia disorder characterized by a bell-shaped thorax, disproportionate short stature, pelvic hypoplasia, dislocatable radial heads and elongated distal fibulae. No acetabular spurs nor phalangeal cone-shaped epiphyses are present and osseous manifestations tend to normalize with age. There have been no further descriptions in the literature since 1988.



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症例報告を絞り込む



合計: 0 (症例報告)

  


(表示件数)
対応する徴候・症状  遺伝子  変異  キーワード(MeSH)
順位
(類似度)
PMID
(PMCID)
        

徴候・症状リスト(Orphanetデータベースから取得)

    合計: 18

HPO ID 徴候・症状 頻度
HP:0000311 丸い顔 Very frequent (99-80%)
HP:0000773 短い肋骨 Very frequent (99-80%)
HP:0000774 狭い胸郭 Very frequent (99-80%)
HP:0000944 骨幹端の異常 Very frequent (99-80%)
HP:0001591 ベル型胸 Very frequent (99-80%)
HP:0002162 後部毛髪線低位 Very frequent (99-80%)
HP:0002644 骨盤帯骨の形態異常 Very frequent (99-80%)
HP:0002857 外反膝 Very frequent (99-80%)
HP:0002991 腓骨の異常 Very frequent (99-80%)
HP:0003042 肘脱臼 Very frequent (99-80%)
HP:0003307 前弯 Very frequent (99-80%)
HP:0005019 骨幹の肥厚 Very frequent (99-80%)
HP:0005692 関節過伸展 Very frequent (99-80%)
HP:0008873 不均衡型短肢低身長 Very frequent (99-80%)
HP:0009826 四肢成長不全 Very frequent (99-80%)
HP:0012368 平坦な顔 Very frequent (99-80%)
HP:0000470 短い頸部 Occasional (29-5%)
HP:0001288 歩行障害 Occasional (29-5%)


徴候・症状リスト(症例報告から取得)

    合計: 0

HPO ID 徴候・症状 症例報告数


疾患原因遺伝子リスト(Orphanetデータベースから取得)

    合計: 0

Gene Symbol 遺伝子名 Entrez Gene ID