MeSH Browser

MeSH Supplementary: Progeroid syndrome, neonatal
Unique ID: C536423
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536423
Entry Term(s): Neonatal progeroid syndrome; Wiedemann-Rautenstrauch syndrome
Heading Mapped to: *Fetal Growth Retardation; *Progeria
Frequency: 26
Note: A rare syndrome characterized by prenatal growth redardation, a failure to thrive, short stature, premature ageing (progeria), hypotonia, and intellectual disability. OMIM: 264090
Date of Entry: 2010/08/25
Revision Date: 2016/09/29

Progeroid syndrome, neonatal MeSH Supplementary Concept Data 2024