Acheiropodia

An extremely rare developmental disorder characterized by bilateral, congenital and complete amputation of the distal extremities (amputation of distal epiphysis of the humerus, distal portion of the tibial diaphysis, aplasia of the radius, ulna, fibula) and aplasia of hands and feet (aplasia of carpal, metacarpal, tarsal, metatarsal and phalangeal bones). Rarely, an ectopic bone can be found at the distal end of the humerus. No other systemic manifestations have been reported and the disorder follows an autosomal recessive pattern of inheritance.



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症例報告を絞り込む



合計: 1 (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)
1
(43.6%)
11582532
[Femur-fibula-ulna (FFU) complex in the 33rd week of gestation: ultrasonography, radiology, pathology and differential diagnosis. Case report].
Guschmann M, Becker R, Urban M, Entezami M, Hese S, Vogel M.
Klin Padiatr. 2001;213(5):301-5.
奇肢症
ヒト 出生前超音波検査 剖検 大腿骨 妊娠 妊娠第三期 胎児 腓骨 鑑別診断
        

徴候・症状リスト(Orphanetデータベースから取得)

    合計: 8

HPO ID 徴候・症状 頻度
HP:0000944 骨幹端の異常 Very frequent (99-80%)
HP:0002990 腓骨無形成 Very frequent (99-80%)
HP:0003974 橈骨欠損 Very frequent (99-80%)
HP:0003982 尺骨欠損 Very frequent (99-80%)
HP:0004050 手欠損 Very frequent (99-80%)
HP:0005792 短い上腕骨 Very frequent (99-80%)
HP:0005930 骨端の異常 Very frequent (99-80%)
HP:0009813 上肢アザラシ肢 Very frequent (99-80%)


徴候・症状リスト(症例報告から取得)

    合計: 1

HPO ID 徴候・症状 症例報告数
HP:0025410 Splenogonadal fusion 1


疾患原因遺伝子リスト(Orphanetデータベースから取得)

    合計: 1

Gene Symbol 遺伝子名 Entrez Gene ID
LMBR1 limb development membrane protein 1 64327