MeSH Browser

MeSH Supplementary: Pierre Robin Sequence with Facial and Digital Anomalies
Unique ID: C564078
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564078
Entry Term(s): Chitayat Meunier Hodgkinson syndrome; Robin sequence with facial and digital anomalies
Registry Number: 0
Heading Mapped to: Fingers / *abnormalities; *Pierre Robin Syndrome; *Facies
Frequency: 1
Note: digital features include tapering fingers, hyperconvex nails, clinodactyly of the fifth fingers, and short distal phalanges; retrognathia, high forehead, and frontal bossing are also observed; OMIM: 311895
Date of Entry: 2012/11/05
Revision Date: 2017/10/19

Pierre Robin Sequence with Facial and Digital Anomalies MeSH Supplementary Concept Data 2024