From Wikipedia, the free encyclopedia
Zori Stalker Williams syndrome is a rare syndrome associated with a range of diseases and symptoms such as Pectus excavatum, macrocephaly and dysplastic nails, familial short stature, developmental delay and distinctive facies.[1][2] Further signs are known to be associated with this syndrome.[3]
The name originates from the researchers who first defined and noticed the syndrome and its clinical signs.[4]
It is believed that the syndrome is inherited in an autosomal dominant pattern, though there has been no new research undertaken for this rare disease.[4]
Zori Stalker Williams syndrome has an autosomal dominant pattern of
inheritance.
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