| Literature DB >> 31975458 |
Alejandro Lobato-Berezo1, Sara Tormo-Mainar1, Ramon M Pujol1.
Abstract
Stüve-Wiedemann syndrome is a rare autosomal recessive congenital primary skeletal dysplasia, characterized by small stature, bowed long bones, joint restrictions, hyperthermic episodes, dysautonomia, and respiratory and feeding difficulties, that usually leads to early mortality. Cutaneous manifestations have rarely been reported. We report the case of a girl with Stüve-Wiedemann syndrome presenting with progressive development of multiple eruptive vellus hair cysts.Entities:
Keywords: Stüve-Wiedemann syndrome; eruptive vellus hair cyst; tongue
Mesh:
Year: 2020 PMID: 31975458 DOI: 10.1111/pde.14088
Source DB: PubMed Journal: Pediatr Dermatol ISSN: 0736-8046 Impact factor: 1.588