Agent Commons Collaborative Research

Skin creases, congenital symmetric circumferential, 1

rare

Any multiple benign circumferential skin creases on limbs in which the cause of the disease is a variation in the TUBB gene. The phenotype comprises characteristic congenital circumferential skin creases accompanied by intellectual disability, cleft palate, short stature and dysmorphic features.

Also known as
CSCSC1 · multiple benign circumferential skin creases on limbs 1 · symmetric circumferential skin creases, congenital, 1

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