Dermatopathia pigmentosa reticularis
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 http://www.orphadata.org. Data version December 2023
Newly diagnosed with
Dermatopathia pigmentosa reticularis?
Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.
Advocacy Organizations
National Foundation for Ectodermal Dysplasias
The NFED mission is to empower and connect those touched by ectodermal dysplasias through education, support and research.
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
For a list of clinical trials in this disease area, please click here.