Literature DB >> 31975458

Stüve-Wiedemann syndrome with multiple eruptive vellus hair cysts and clefted tongue.

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.
© 2020 Wiley Periodicals, Inc.

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


  1 in total

Review 1.  Clinical overview and outcome of the Stuve-Wiedemann syndrome: a systematic review.

Authors:  Hélène Warnier; Christophe Barrea; Sarah Bethlen; Isabelle Schrouff; Julie Harvengt
Journal:  Orphanet J Rare Dis       Date:  2022-04-23       Impact factor: 4.303

  1 in total

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