Other Names for this Disease
- Ichtyosis, Brittle hair, Intellectual impairment, Decreased fertility, and Short stature
- Tay syndrome
- Trichothiodystrophy with congenital ichtyosis
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Tay syndrome is a rare genetic disorder characterized by congenital ichthyosis (dry, fish-like scaly skin present at birth) and abnormal brittle hair (trichothiodystrophy).
Last updated: 7/30/2013
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- The Online Mendelian Inheritance in Man (OMIM) is an catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- PubMed is a searchable database of medical literature and lists journal articles that discuss IBIDS syndrome. Click on the link to view a sample search on this topic.