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Progeroid syndrome, neonatal MeSH Supplementary Concept Data 2024


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
Registry Number
0
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 Preferred
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