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Артрогрипозно-гіперкератозний синдром, летальна форма

ORPHA:1485· ICD-10 Q68.8· Arthrogryposis-hyperkeratosis syndrome, lethal form

Визначення(English summary)

A rare arthrogryposis syndrome characterized by the association of multiple congenital joint contractures (of the large joints, fingers and toes) and hyperkeratosis (i.e. thick, scaling and fissured skin), with death occurring in early infancy. There have been no further reports in the literature since 1993.

Поширеність
<1 / 1 000 000
Успадкування
Unknown
Вік початку
Neonatal