Atypical Werner syndrome

MONDO:0019321

A 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.

Also known as: atypical progeroid syndrome

1 clinical trial for this condition and its sub-types, 0 tagged with Atypical Werner syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Disorder of development or morphogenesis (5170) ↑ Laminopathy (25)

Including sub-types (1) Tagged with Atypical Werner syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.