Dermatopathia pigmentosa reticularis

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A rare genetic ectodermal dysplasia characterized by a widespread early-onset reticulate hyperpigmentation that persists throughout life mild diffuse non-cicatricial alopecia and onychodystrophy. There are no dental anomalies. Patients may also present with adermatoglyphia palmoplantar hyperkeratosis acral dorsal blistering and hypohidrosis or hyperhidrosis.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on Data version July 2024

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Dermatopathia pigmentosa reticularis?

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