An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review.

Xu, Duojiao; Guo, Yujiao; Qi, Zhan; Hao, Chanjuan; Yu, Guoxia

Xu, Duojiao; Guo, Yujiao; Qi, Zhan; Hao, Chanjuan; Yu, Guoxia.

Afiliación

Xu D; Department of Stomatology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Guo Y; Department of Stomatology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Qi Z; Beijing Key Laboratory for Genetics of Birth Defects, Beijing Pediatric Research Institute, MOE Key Laboratory of Major Diseases in Children, Rare Disease Center, National Center for Children's Health, Beijing Children's Hospital, Capital Medical University, Beijing, China.
Hao C; Beijing Key Laboratory for Genetics of Birth Defects, Beijing Pediatric Research Institute, MOE Key Laboratory of Major Diseases in Children, Rare Disease Center, National Center for Children's Health, Beijing Children's Hospital, Capital Medical University, Beijing, China.
Yu G; Department of Stomatology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.

Heliyon ; 9(10): e20857, 2023 Oct.

Article en En | MEDLINE | ID: mdl-37916118

Palabras clave

Congenital micrognathia; Dyspnea; Hutchinson-Gilford progeria syndrome; LMNA mutation; Mandibular distraction osteogenesis

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Heliyon Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

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