Werner syndrome

Werner syndrome (WS) is a rare inherited syndrome characterized by premature aging with onset in the third decade of life and with cardinal clinical features including bilateral cataracts, short stature, graying and thinning of scalp hair, characteristic skin disorders and premature onset of additional age-related disorders.

Micromelia

The presence of abnormally small extremities.


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PMID (PMCID)
27530878
 MALE Infant
Tibial hypoplasia with a bifid tibia: an unclassified tibial hemimelia.
Shah K, Shah H.
BMJ Case Rep. 2016;2016:.
The tibial hemimelia is usually described with preaxial mirror polydactyly, split hand/foot syndrome-ectrodactyly, polydactyly-triphalangeal thumb syndrome (Werner syndrome) and micromelia-trigonal brachycephaly syndrome.