Hereditary symmetrical dyschromatosis (Q98794): Difference between revisions
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CID11:ID_1506483461 | |||||||||||||||
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dki-india-ID_1506483461 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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Latest revision as of 15:24, 16 August 2026
Hereditary symmetrical dyschromatosis is an autosomal recessive pigmentary disorder characterised by hypo- and hyperpigmented macules affecting predominantly the dorsal surfaces of the hands and feet. On the face the lesions resemble ephelides and no hypopigmentation appears. The condition is commoner in individuals of oriental origin. It develops during infancy and early childhood and persists into adulthood.
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| default for all languages | ID_1506483461 |
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| English | Hereditary symmetrical dyschromatosis |
Hereditary symmetrical dyschromatosis is an autosomal recessive pigmentary disorder characterised by hypo- and hyperpigmented macules affecting predominantly the dorsal surfaces of the hands and feet. On the face the lesions resemble ephelides and no hypopigmentation appears. The condition is commoner in individuals of oriental origin. It develops during infancy and early childhood and persists into adulthood. |
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CID11:ID_1506483461
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dki-india-ID_1506483461
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Concluído
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15 August 2026
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