Article

Craniofacial And Dentoalveolar Morphology In Individuals With Prader-Willi Syndrome: A Case-Control Study.

2021-08-12

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> Prader-Willi syndrome (PWS) is a complex multisystem genetic disorder with distinct genetic and clinical features. Among other clinical symptoms, PWS is characterized by severe infantile hypotonia with feeding problems, childhood onset hyperphagia, obesity, scoliosis, short stature combined with growth hormone deficiency and developmental delay. PWS is associate...

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Literature Corpus work: 3924b26f-63a4-5376-9a7b-16659928c8c8
DOI: 10.21203/rs.3.rs-592523/v1

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