MeSH Browser

MeSH Supplementary: Ruvalcaba Churesigaew Myhre syndrome
Unique ID: C537190
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537190
Registry Numbers: 0
Heading Mapped to: *Progeria
Frequency: 0
Note: Onset of senility in the early teens, atrophic skin, hypogonadism, retinal and vascular sclerosis
Source: Clin Pediatr (Phila). 1977;16(3):248-52
Date of Entry: 2010/08/25
Revision Date: 2010/08/25

Ruvalcaba Churesigaew Myhre syndrome MeSH Supplementary Concept Data 2025