Böök syndrome

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Böök syndrome

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 March 2024

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Böök syndrome?

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