Hereditary symmetrical dyschromatosis (Q98794): Difference between revisions
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| description / pt-br | description / pt-br | ||
Discromatose simétrica hereditária é um transtorno pigmentar autossômico recessivo caracterizado por máculas hipo e hiperpigmentadas que afetam predominantemente as superfícies dorsais de mãos e pés. Na face as lesões assemelham-se a efélides e não aparece hipopigmentação. A condição é mais comum em indivíduos de origem oriental. Desenvolve-se durante a primeira infância e a infância e persiste na idade adulta. | |||
| description / en | description / en | ||
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. | |||
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| 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. |
