Dermatopathia pigmentosa reticularis (also known as "Dermatopathia pigmentosa reticularis hyperkeratotica et mutilans," "Dermatopathia pigmentosa reticularis hypohidotica et atrophica," and "Dermatopathic pigmentosa reticularis") is a rare, autosomal dominant congenital disorder that is a form of ectodermal dysplasia. Dermatopathia pigmentosa reticularis is composed of the triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy.
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- Dermatopathia pigmentosa reticularis (also known as "Dermatopathia pigmentosa reticularis hyperkeratotica et mutilans," "Dermatopathia pigmentosa reticularis hypohidotica et atrophica," and "Dermatopathic pigmentosa reticularis") is a rare, autosomal dominant congenital disorder that is a form of ectodermal dysplasia. Dermatopathia pigmentosa reticularis is composed of the triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy.
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- Dermatopathia pigmentosa reticularis
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- Dermatopathia pigmentosa reticularis (also known as "Dermatopathia pigmentosa reticularis hyperkeratotica et mutilans," "Dermatopathia pigmentosa reticularis hypohidotica et atrophica," and "Dermatopathic pigmentosa reticularis") is a rare, autosomal dominant congenital disorder that is a form of ectodermal dysplasia. Dermatopathia pigmentosa reticularis is composed of the triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy.
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- Dermatopathia pigmentosa reticularis
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- Dermatopathia pigmentosa reticularis
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