2020
DOI: 10.17816/2686-8997-2020-1-3-188-196
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Noonan-like syndrome with loose anagen hair: three clinical cases

Abstract: Noonan-like syndrome with loose anagen hair is a rare inherited disease caused by heterozygous mutation in theSHOC2gene. The disease was first described in 1991. The main clinical manifestations of the disease are phenotype features similar to those observed in Noonan syndrome: orbital hypertelorism, eyelid ptosis, low-set, and posteriorly rotated auricles, as well as skin and hair lesions, development delay, loose anagen hair, cardiovascular disorders, and mental retardation. It has an autosomal dominant mode… Show more

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