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disease > genetic disease > hereditary disease > Jackson-Lawler pachyonychia
disease > congenital disease > malformation > ectodermal dysplasia > Jackson-Lawler pachyonychia
disease > stomatology > dental disease > ectodermal dysplasia > Jackson-Lawler pachyonychia
disease > dysplasia > ectodermal dysplasia > Jackson-Lawler pachyonychia
disease > genetic disease > hereditary disease > ectodermal dysplasia > Jackson-Lawler pachyonychia
... > disease > skin appendages disease > skin disease > sweat gland disease > ectodermal dysplasia > Jackson-Lawler pachyonychia
disease > skin appendages disease > hypotrichosis > ectodermal dysplasia > Jackson-Lawler pachyonychia
disease > skin appendages disease > nail disease > Jackson-Lawler pachyonychia
disease > skin appendages disease > skin disease > dyskeratosis > Jackson-Lawler pachyonychia

Terme préférentiel

Jackson-Lawler pachyonychia  

Définition

  • 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. (Wikipedia)

Concept générique

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-DVC9HSRR-7

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