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Progeroid syndrome, neonatal [Supplementary Concept]

A rare syndrome characterized by prenatal growth redardation, a failure to thrive, short stature, premature ageing (progeria), hypotonia, and intellectual disability. OMIM: 264090

Date introduced: August 25, 2010

MeSH Unique ID: C536423

Heading Mapped to:

Entry Terms:

  • Neonatal progeroid syndrome
  • Wiedemann-Rautenstrauch syndrome

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