Synonyms: Bitemporal aplasia cutis congenita | Brauer syndrome | FFDD type I | FFDD1 | Focal facial dermal dysplasia 1, Brauer type | Focal facial dermal dysplasia type 1
Focal facial dermal dysplasia type I (FFDD1) also known as Brauer syndrome is a focal facial dysplasia (FFDD; see this term) characterized by congenital bitemporal cutis aplasia.
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 April 2026
Newly diagnosed with
Focal facial dermal dysplasia type I?
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Advocacy Organizations
National Foundation for Ectodermal Dysplasias
Together, we enrich the lives of people affected by ectodermal dysplasias by fostering community, providing education and support, and driving advocacy and groundbreaking research—creating a brighter future for all.
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Clinical Trials
For a list of clinical trials in this disease area, please click here.