Aplasia cutis congenita
A rare skin disorder characterized by localized absence of skin that is usually located on the scalp but can occur anywhere on the body including the face trunk and extremities. Aplasia cutis congenita (ACC) may occasionally be associated with other anomalies.
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 September 2023.
Newly diagnosed with
Aplasia cutis congenita?
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Advocacy Organizations
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.