Tay syndrome

IBIDS syndrome, Trichothiodystrophy with congenital ichtyosis

Overview

Type of disease: Rare conditions

Tay syndrome is a rare genetic disorder characterized by congenital ichthyosis (dry, fish-like scaly skin present at birth) and abnormal brittle hair (trichothiodystrophy).
Source: Genetic and Rare Diseases Information Center (GARD), supported by ORDR-NCATS and NHGRI.

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