![Jordan's Syndrome on Twitter: "Happy Midsummer from our family from Sweden!! #ppp2r5d #jordanssyndrome #jordansguardianangels #midsummer2018 https://t.co/i7g4n9WuDl" / Twitter Jordan's Syndrome on Twitter: "Happy Midsummer from our family from Sweden!! #ppp2r5d #jordanssyndrome #jordansguardianangels #midsummer2018 https://t.co/i7g4n9WuDl" / Twitter](https://pbs.twimg.com/media/DgULVb8UwAAYm-V.jpg)
Jordan's Syndrome on Twitter: "Happy Midsummer from our family from Sweden!! #ppp2r5d #jordanssyndrome #jordansguardianangels #midsummer2018 https://t.co/i7g4n9WuDl" / Twitter
El lenguaje expresivo está afectado debido a la hipotonia (bajo tono muscular) para poder articular palabras necesitamos de los musculos de nuestra boca es por ello la dificultad, con terapias podremos tener
![Jordan's Syndrome on Twitter: "Meet Katelyn from California, USA https://t.co/VJ1pfXTZwJ #ppp2r5d #jordanssyndrome #meetourfamily #raregenetics https://t.co/dNnhJdZ81e" / Twitter Jordan's Syndrome on Twitter: "Meet Katelyn from California, USA https://t.co/VJ1pfXTZwJ #ppp2r5d #jordanssyndrome #meetourfamily #raregenetics https://t.co/dNnhJdZ81e" / Twitter](https://pbs.twimg.com/media/DLdb-TZW4AArN28.jpg)
Jordan's Syndrome on Twitter: "Meet Katelyn from California, USA https://t.co/VJ1pfXTZwJ #ppp2r5d #jordanssyndrome #meetourfamily #raregenetics https://t.co/dNnhJdZ81e" / Twitter
![PDF) PPP2R5D-Related Intellectual Disability and Neurodevelopmental Delay: A Review of the Current Understanding of the Genetics and Biochemical Basis of the Disorder PDF) PPP2R5D-Related Intellectual Disability and Neurodevelopmental Delay: A Review of the Current Understanding of the Genetics and Biochemical Basis of the Disorder](https://i1.rgstatic.net/publication/339361130_PPP2R5D-Related_Intellectual_Disability_and_Neurodevelopmental_Delay_A_Review_of_the_Current_Understanding_of_the_Genetics_and_Biochemical_Basis_of_the_Disorder/links/5e4d3e4b92851c7f7f45c54a/largepreview.png)
PDF) PPP2R5D-Related Intellectual Disability and Neurodevelopmental Delay: A Review of the Current Understanding of the Genetics and Biochemical Basis of the Disorder
![A disorder-related variant (E420K) of a PP2A-regulatory subunit (PPP2R5D) causes constitutively active AKT-mTOR signaling and uncoordinated cell growth - ScienceDirect A disorder-related variant (E420K) of a PP2A-regulatory subunit (PPP2R5D) causes constitutively active AKT-mTOR signaling and uncoordinated cell growth - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S002192582100082X-gr1.jpg)
A disorder-related variant (E420K) of a PP2A-regulatory subunit (PPP2R5D) causes constitutively active AKT-mTOR signaling and uncoordinated cell growth - ScienceDirect
![A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype](https://static-02.hindawi.com/articles/bmri/volume-2021/6661860/figures/6661860.fig.001b.jpg)