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Thrombocytosis in an infant with a TRPV4 mutation: a case report.

Platelets 2020 April 23
Mutations in the calcium channel gene Transient Receptor Potential cation channel subfamily V member 4 ( TRPV4 ) cause autosomal dominant skeletal dysplasia, with phenotypes ranging from mild to perinatal lethality. A recent report detailed enhanced proplatelet formation and increased murine platelet count in the context of TRPV4 activation. No prior reports have described platelet count abnormalities in human TRPV4 disease. Here, we report a case of prolonged thrombocytosis in the context of TRPV4 -associated metatropic dysplasia that was lethal in the infantile period.

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