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Поміняти порядок слів: Синдром фіброматозу ясен-гіпертрихозу

ORPHA:2026· ICD-10 L68.8· Gingival fibromatosis-hypertrichosis syndrome

Визначення(English summary)

A rare autosomal dominant disorder characterized by a generalized enlargement of the gingiva occurring at birth or during childhood that is associated with generalized hypertrichosis developing at birth, during the first years of life, or at puberty and predominantly affecting the face, upper limbs, and midback.

Поширеність
Unknown
Успадкування
Autosomal dominant
Вік початку
Infancy, Neonatal