Böök syndrome

Get in touch with RARE Concierge.

Contact RARE Concierge

A rare autosomal dominant ectodermal dysplasia syndrome characterized by premolar aplasia hyperhidrosis and premature graying of the hair. Additional features may include a narrow palate hypoplastic nails eyebrow anomalies a unilateral simian crease and poorly formed dermatoglyphics.

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 May 2024

Newly diagnosed with
Böök syndrome?

Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.

Get Concierge Help

Advocacy Organizations

Don't see your organization here. Let us know here.

Clinical Trials

For a list of clinical trials in this disease area, please click here.