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Stüve-Wiedemann syndrome with multiple eruptive vellus hair cysts and clefted tongue.
Lobato-Berezo, Alejandro; Tormo-Mainar, Sara; Pujol, Ramon M.
Affiliation
  • Lobato-Berezo A; Department of Dermatology, Hospital del Mar-Parc de Salut Mar, Barcelona, Spain.
  • Tormo-Mainar S; Department of Dermatology, Hospital del Mar-Parc de Salut Mar, Barcelona, Spain.
  • Pujol RM; Department of Dermatology, Hospital del Mar-Parc de Salut Mar, Barcelona, Spain.
Pediatr Dermatol ; 37(2): 381-382, 2020 Mar.
Article in En | MEDLINE | ID: mdl-31975458
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteochondrodysplasias / Tongue Diseases / Exostoses, Multiple Hereditary / Oral Ulcer / Epidermal Cyst / Hair Diseases Limits: Child / Female / Humans Language: En Journal: Pediatr Dermatol Year: 2020 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteochondrodysplasias / Tongue Diseases / Exostoses, Multiple Hereditary / Oral Ulcer / Epidermal Cyst / Hair Diseases Limits: Child / Female / Humans Language: En Journal: Pediatr Dermatol Year: 2020 Document type: Article Affiliation country: