DYRK1A syndrome has been extensively studied primarily with regard to neurologic and other phenotypic features such as skeleton and craniofacial alterations. In the present paper, we aim to highlight unusual anomalies associated with a DYRK1A mutation: a 17-year-old female patient with language and cognitive delay, microcephaly, and an autistic disorder, who was operated upon for spleen torsion with anomalous gut fixation.

Case Report: Gut and spleen anomalies associated with DYRK1A syndrome / Infantino, I; Tocchioni, F; Ghionzoli, M; Coletta, R; Morini, F; Morabito, A. - In: FRONTIERS IN PEDIATRICS. - ISSN 2296-2360. - 10:(2023), pp. 936732-936732. [10.3389/fped.2022.936732]

Case Report: Gut and spleen anomalies associated with DYRK1A syndrome

Morini, F;
2023

Abstract

DYRK1A syndrome has been extensively studied primarily with regard to neurologic and other phenotypic features such as skeleton and craniofacial alterations. In the present paper, we aim to highlight unusual anomalies associated with a DYRK1A mutation: a 17-year-old female patient with language and cognitive delay, microcephaly, and an autistic disorder, who was operated upon for spleen torsion with anomalous gut fixation.
2023
DYRK1A; gut abnormalities; intestinal obstruction; spleen abnormalities; splenectomy
01 Pubblicazione su rivista::01a Articolo in rivista
Case Report: Gut and spleen anomalies associated with DYRK1A syndrome / Infantino, I; Tocchioni, F; Ghionzoli, M; Coletta, R; Morini, F; Morabito, A. - In: FRONTIERS IN PEDIATRICS. - ISSN 2296-2360. - 10:(2023), pp. 936732-936732. [10.3389/fped.2022.936732]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1701738
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