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Atypical Werner syndrome

Disease Export to PDF
Name:
Atypical Werner syndrome
Description:
An heterogeneous group of cases that are clinically diagnosed as Werner syndrome (WS) but do not carry WRN gene mutations. Similar to classical WS caused by WRN mutations, patients generally exhibit an aged appearance and common age-related disorders at earlier ages compared to the general population.
ORPHAcode:
79474
Synonyms:
Atypical progeroid syndrome
XREF(s):
Orphanet
ICD-10
Analyte(s):
LMNA
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14