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・ Acheilognathus polyspinus
・ Acheilognathus rhombeus
・ Acheilognathus signifer
・ Acheilognathus somjinensis
・ Acheilognathus tabira
・ Acheilognathus tabira erythropterus
・ Acheilognathus tabira jordani
・ Acheilognathus tabira nakamurae
・ Acheilognathus tabira tabira
・ Acheilognathus tabira tohokuensis
・ Acheilognathus taenianalis
・ Acheilognathus tonkinensis
・ Acheilognathus typus
・ Acheilognathus yamatsutae
・ Acheiria
Acheiropodia
・ Acheiropoieta
・ Acheiropoietos Monastery
・ Achel Abbey
・ Achel Brewery
・ Achelata
・ Acheleia
・ Achelia
・ Achelois
・ Acheloma
・ Acheloos
・ Acheloos (municipality)
・ Acheloos Painter
・ Acheloos TV
・ Achelous


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Acheiropodia : ウィキペディア英語版
Acheiropodia

Acheiropodia (ACHP), also known as Horn-Kolb Syndrome, Acheiropody and Aleijadinhos (Brazilian type), is an autosomal recessive disorder that results in hemimelia, a lack of formation of the distal extremities.
This is a congenital defect which consists of bilateral amputations of the distal upper and lower extremities, as well as aplasia of the hands and feet. It was first discovered and is prevalent almost exclusively in Brazil.
==Genetics==

ACHP has been associated with a mutation in the ''LMBR1'' gene. The disorder is inherited in an autosomal recessive manner.〔 This means the defective gene responsible for the disorder is located on an autosome, and two copies of the defective gene (one inherited from each parent) are required in order to be born with the disorder. The parents of an individual with an autosomal recessive disorder both carry one copy of the defective gene, but usually do not experience any signs or symptoms of the disorder.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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