" /> Hereditary symmetrical dyschromatosis - CISMeF





Preferred Label : Hereditary symmetrical dyschromatosis;

ICD-11 definition : Hereditary symmetrical dyschromatosis is an autosomal recessive pigmentary disorder characterized 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.;

ICD-11 synonym : Reticulate acropigmentation of Dohi;

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Position du mot-clé dans l'(les) arborescence(s) : arborescence

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Hereditary symmetrical dyschromatosis is an autosomal recessive pigmentary disorder characterized 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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30/07/2025


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