Ectodermal dysplasia with congenital adermatoglyphia (Basan syndrome): Report of two cases presenting with extensive congenital milia.
Pediatr Dermatol
; 38(2): 530-532, 2021 Mar.
Article
in En
| MEDLINE
| ID: mdl-33486784
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.
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Skin Diseases, Genetic
/
Ectodermal Dysplasia
/
Nails, Malformed
Type of study:
Diagnostic_studies
Limits:
Humans
Language:
En
Journal:
Pediatr Dermatol
Year:
2021
Document type:
Article
Affiliation country:
Spain