Article
Usmani-Riazuddin syndrome can have a recognizable phenotype: Report of a novel AP1G1 variant.
Clinical genetics - 1 Jul 2024
Gnazzo Maria, Pascolini Giulia, Parlapiano Giovanni, Petrizzelli Francesco, Perrino Daniele, Porco Luigina, Bartuli Andrea, Novelli Antonio, Baban Anwar
Abstract excerpt
Usmani-Riazuddin syndrome (USRISR, MIM# 619548; USRISD, MIM#619467) is a very rare genetic condition. recently associated with deleterious variants in AP1G1 (MIM* 603533). It is characterized by multisystemic involvement including intellectual disability, speech and developmental delay, behavioral anomalies, muscular tone disorders, seizures, limb defects, and unspecified facial gestalt. In this report, we...
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