MeSH Browser

MeSH Supplementary: Penttinen-Aula syndrome
Unique ID: C536653
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536653
Entry Term(s): Premature Aging Syndrome, Penttinen Type; Premature aging syndrome Penttinen type
Registry Number: 0
Heading Mapped to: *Progeria; *Limb Deformities, Congenital; *Acro-Osteolysis
Frequency: 9
Note: Prematurely aged appearance, delayed bone maturation, acro-osteolysis, and brachydactyly
Date of Entry: 2010/08/25
Revision Date: 2012/12/03

Penttinen-Aula syndrome MeSH Supplementary Concept Data 2024