Basan Syndrome

Common Name(s)

Basan Syndrome

Complete congenital absence of dermatoglyphs is a rare syndrome characterized by autosomal dominant inheritance of the lack of ridges on palms and soles, neonatal acral blisters and facial milia, adult traumatic blistering and fissuring, absent or reduced sweating of palms and soles, and contracture of digits. Additional features may include single palmar transverse crease, palmoplantar keratoderma, and nail grooving (summary by {9:Limova et al., 1993}).
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Basan Syndrome" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Basan Syndrome" returned 1 free, full-text research articles on human participants. First 3 results:

Genome-wide linkage analysis and whole-genome sequencing identify a recurrent SMARCAD1 variant in a unique Chinese family with Basan syndrome.
 

Author(s): Ming Li, Jianbo Wang, Zhenlu Li, Jia Zhang, Cheng Ni, Ruhong Cheng, Zhirong Yao

Journal: Eur. J. Hum. Genet.. 2016 Aug;24(9):1367-70.

 

Basan syndrome is a rare autosomal dominant genodermatosis, characterized by rapidly healing congenital acral bullae, congenital milia and lack of fingerprints. A mutation in the SMARCAD1 gene was recently reported to cause Basan syndrome in one family. Here, we present a large Chinese ...

Last Updated: 12 Aug 2016

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Reviews from the PubMed Database

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The terms "Basan Syndrome" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.