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Basan syndrome is a rare autosomal dominant genodermatosis, characterized by rapidly healing congenital acral bullae, congenital milia and adermatoglyphia (lack of finger and toeprints). This type of ectodermal dysplasia has… Click to show full abstract
Basan syndrome is a rare autosomal dominant genodermatosis, characterized by rapidly healing congenital acral bullae, congenital milia and adermatoglyphia (lack of finger and toeprints). This type of ectodermal dysplasia has been infrequently reported in the literature. A pathogenic mutation in the SMARCAD1 gene has been demonstrated to cause this rare disorder.
Keywords:
basan syndrome;
ectodermal dysplasia;
dysplasia congenital;
congenital milia
Journal Title: Pediatric Dermatology
Year Published: 2021
Link to full text (if available)
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Journal Title: Pediatric Dermatology
Year Published: 2021
Link to full text (if available)
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recommendations!