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Tay syndrome
Tay syndrome is a recessive hereditary disease characterised by trichothiodystrophy (sulfur-deficient brittle hair) with photosensitivity, ichthyosiform erythroderma (fish-like scales on skin), dystrophic (abnormal) finger and toe-nails, progeria-like faces (prematurely aged looking face), growth and mental retardation, infertility and variable other defects. Additional recommended knowledgeIt is named after Dr. Tay Chong Hai, a Singaporean doctor who discovered and subsequently published a paper on it in 1971. Dr. Tay is the first doctor in South East Asia to be honoured by having a disease named after him. The Tay syndrome should not be confused with the Tay-Sachs disease. Tay syndrome is synonymous with:
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This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Tay_syndrome". A list of authors is available in Wikipedia. |