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Fibrous dysplasia in cardio-facio-cutaneous syndrome: A case report and review of literature.
Dong, Xiaoao; Png, Nicholas C Y; Fortier, Marielle V; Lim, Jiin Ying; Wong, Kenneth P L; Choo, Jonathan T L; Tan, Ene Choo; Jamuar, Saumya Shekhar.
Afiliação
  • Dong X; Department of Paediatrics, KK Women's and Children's Hospital, Singapore.
  • Png NCY; Department of Diagnostic and Interventional Radiology, KK Women's and Children's Hospital, Singapore.
  • Fortier MV; Department of Diagnostic and Interventional Radiology, KK Women's and Children's Hospital, Singapore.
  • Lim JY; Department of Paediatrics, KK Women's and Children's Hospital, Singapore.
  • Wong KPL; SingHealth Duke-NUS Genomic Medicine Centre, Singapore.
  • Choo JTL; Department of Paediatric Orthopaedics, KK Women's and Children's Hospital, Singapore.
  • Tan EC; Department of Cardiology, KK Women's and Children's Hospital, Singapore.
  • Jamuar SS; KK Research Centre, KK Women's and Children's Hospital, Singapore.
Am J Med Genet A ; 188(9): 2732-2737, 2022 09.
Article em En | MEDLINE | ID: mdl-35801299
Cardio-facio-cutaneous (CFC) syndrome (OMIM #:115150, 615278, 615279, 615280) is a rare genetic condition caused by variants in the RAS/mitogen-activated protein kinase (MAPK) signal transduction pathway. Up to 75% of cases are caused by mutations in the BRAF gene, whereas KRAS gene mutation has only been reported in <2% of cases. CFC syndrome is characterized by cardiac abnormalities, distinctive craniofacial dysmorphism, and various cutaneous abnormalities. Musculoskeletal and orthopedic manifestations are also prevalent in patients with CFC syndrome, among which the most common are skeletal deformities and joint laxities. Dysplastic bone disorders, on the other hand, have not been reported in CFC syndrome before. We report on a case of symmetrical polyostotic fibrous dysplasia (FD) in a patient with CFC syndrome with the KRAS(NM_004985.5):c.57G>C; p.Leu19Phe variant. The FDs were incidentally picked up, and patient was conservatively managed and remained asymptomatic on follow-up. The same variant was reported previously in a patient with Oculoectodermal Syndrome (OES), who developed polyostotic non-ossifying fibroma (NOF). This case explores FD as a possible new clinical feature of CFC syndrome, and when linked to the historical case of OES, explores whether the KRAS(NM_004985.5):c.57G>C; p.Leu19Phe mutation may potentially contribute to the development of dysplastic bone lesions in patients with this particular mutation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Displasia Ectodérmica / Cardiopatias Congênitas Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Singapura

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Displasia Ectodérmica / Cardiopatias Congênitas Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Singapura