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Ectodermal Dysplasia
Clinical trial pipeline · Data from ClinicalTrials.gov
See which Ectodermal Dysplasia trials may be worth asking aboutClinical trial pipeline · Data from ClinicalTrials.gov
See which Ectodermal Dysplasia trials may be worth asking aboutNorth America
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The goal of this research study is to identify genes and regulatory elements on chromosomes that cause ACC. The investigators also study tissue samples from pat…
Ectodermal dysplasia is a rare inherited condition that affects structures derived from the ectoderm, including teeth, skin, hair, and sweat glands. Dental find…
The goal of this observational study is to conduct a prospective assessment of the individual Burden of 9 rare skin diseases to assess disability in the broades…
The goal of this observational study is to create a single macro registry system with data collection on common clinical features, grouping the different rare d…
The aim of the CDH1-associated Blepharocheilodontic Syndrome (BCDS) registry is to better characterize the clinical features of this condition and exploring whe…
CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, i…
Focal dermal hypoplasia, or Goltz syndrome, results from genetic changes, or mutations in the PORCN gene located on the X chromosome. This neurodevelopmental di…
Epidermal growth factor receptor (EGFR) signaling plays a key role in regulating epidermal cell proliferation, survival, and differentiation. Keratins form a sc…