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Am J Med Genet A ; 194(8): e63634, 2024 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-38619072

RESUMO

Feeding difficulties, aspiration, and failure to thrive in infancy are commonly seen in patients with Prader-Willi Syndrome (PWS) and attributed to hypotonia. Patients with PWS and laryngeal clefts were identified by review of medical records at three tertiary care children's hospitals between 2017 and 2022. We present three patients with PWS with feeding difficulties who were also found to have laryngeal clefts which likely contributed to their feeding difficulties. Additional factors such as airway anomalies should be considered in patients with PWS, especially when swallowing dysfunction, dysphagia, or abnormal swallow evaluations are present.


Assuntos
Laringe , Hipotonia Muscular , Síndrome de Prader-Willi , Humanos , Síndrome de Prader-Willi/complicações , Síndrome de Prader-Willi/diagnóstico , Síndrome de Prader-Willi/genética , Síndrome de Prader-Willi/patologia , Hipotonia Muscular/genética , Hipotonia Muscular/patologia , Feminino , Masculino , Lactente , Laringe/anormalidades , Laringe/patologia , Laringe/fisiopatologia , Pré-Escolar , Transtornos de Deglutição/etiologia , Transtornos de Deglutição/diagnóstico , Anormalidades Congênitas
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