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g children's hospitalization affects the level of agreement between reports on their HRQOL.An amendment to this paper has been published and can be accessed via the original article. Melnick-Needles syndrome (MNS) is an extremely rare osteochondrodysplasia caused by a mutation of FLNA, the gene encoding filamin A. MNS is inherited in an X-linked dominant manner. In this study, we describe three members of the same family with MNS, who exhibited different phenotypic severity despite having an identical FLNA gene mutation. The patient was
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