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Periorbital hyperpigmentation. An overlooked genetic disorder of pigmentation

Richard M. Goodman

Open publisher page 38 citations

Abstract

This is the first English report of a family with a genetically determined form of hyperpigmentation involving the periorbital area. Only two other reports of this trait have been found in the European literature. Twenty-two affected members in six generations were noted to have this type of hyperpigmentation. Various clinical and genetic aspects of their autosomal dominant trait are discussed.

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What this paper is about

This is the first English report of a family with a genetically determined form of hyperpigmentation involving the periorbital area. Only two other reports of this trait have been found in the European literature. Twenty-two affected members in six generations were noted to have this type of hyperpigmentation. Various clinical and genetic aspects of their autosomal dominant trait are discussed.

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OpenAlex reports 38 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

This is the first English report of a family with a genetically determined form of hyperpigmentation involving the periorbital area. Only two other reports of this trait have been found in the European literature. Twenty-two affected members in six generations were noted to have this type of hyperpigmentation. Various clinical and genetic aspects of their autosomal dominant trait are discussed.

Key concepts: Hyperpigmentation, Pigmentation disorder, Medicine, Dermatology, Trait, Skin hyperpigmentation, Genetics, Biology

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