A Patient With Schimmelpenning Syndrome and Mosaic KRAS Mutation.


Journal

The Journal of craniofacial surgery
ISSN: 1536-3732
Titre abrégé: J Craniofac Surg
Pays: United States
ID NLM: 9010410

Informations de publication

Date de publication:
Jan 2019
Historique:
pubmed: 6 11 2018
medline: 2 3 2019
entrez: 6 11 2018
Statut: ppublish

Résumé

Schimmelpenning syndrome is a neurocutaneous disorder characterized by craniofacial nevus sebaceus that fall along embryonic cutaneous lines and tend to be associated with neurological, ocular, skeletal, and vascular abnormalities. We report a child with extensive nevus sebaceus of the scalp, face, and thorax and other unusual physical findings who was found to have a mosaic mutation of KRAS c.35G>A p.12D pathognomonic of Schimmelpenning syndrome.

Identifiants

pubmed: 30394973
doi: 10.1097/SCS.0000000000004887
doi:

Substances chimiques

KRAS protein, human 0
Proto-Oncogene Proteins p21(ras) EC 3.6.5.2

Types de publication

Case Reports Journal Article

Langues

eng

Pagination

184-185

Auteurs

Benjamin J Mitchell (BJ)

Georgetown University School of Medicine.

Gary F Rogers (GF)

Division of Plastic Surgery, Children's National Health System, Washington, DC.

Benjamin C Wood (BC)

Division of Plastic Surgery, Children's National Health System, Washington, DC.

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Classifications MeSH