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Clin Case Rep ; 11(8): e7753, 2023 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-37529132

RESUMO

We report two, genotypically identical but phenotypically distinct cases of Schaaf-Yang syndrome and propose the early use of Genome Sequencing in patients with nonspecific presentations to facilitate the early diagnosis of children with rare genetic diseases and improve overall health care outcomes.

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