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Jackson-Lawler type pachyonychia congenita : ウィキペディア英語版
Pachyonychia congenita

Pachyonychia congenita is an autosomal dominant skin disorder.
== Classification ==
Pachyonychia congenita may be divided into the following types:〔Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.〕
* ''Pachyonychia congenita type I'' (also known as "Jadassohn–Lewandowsky syndrome"〔) is an autosomal dominant keratoderma that principally involves the plantar surfaces, but also with nails changes that may be evident at birth but more commonly develop within the first few months of life.〔〔James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0-7216-2921-0.〕
* ''Pachyonychia congenita type II'' (also known as "Jackson–Lawler pachyonychia congenita," and "Jackson–Sertoli syndrome") is an autosomal dominant keratoderma presenting with a limited focal plantar keratoderma that may be very minor, with nails changes that may be evident at birth, but more commonly develop within the first few months of life.〔〔

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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