In March, the American Journal of Medecine Genetics published an article showing that a mutation on the gene PTDSS1 leads to a very rare type of Cutis Laxa : Lenz-Majewski Syndrome (LMS) . It includes Cutis Laxa with growth delay, dwarfism and intellectual delay. According to this study of 3 cases, this is a new type of […]
https://www.cutislaxa.org/wp-content/uploads/2017/07/gene-small.jpg169300Marie-Claudehttp://www.cutislaxa.org/wp-content/uploads/2017/12/NEW-LOGO-CLI-4.pngMarie-Claude2018-03-31 15:35:052018-09-18 15:37:37A New Type of Cutis Laxa
As of today, 12 different mutations have been identified leading to Cutis Laxa. That is why Cutis Laxa classification will soon be reviewed. Elastine (ELN) (2 mutations) – ADCL Fibuline5 (FBLN5) – ARCL1A Fibuline4 (FBLN4) – ARCL1B LTBP4 – ARCL1C ATP6V0A2 – ARCL2A PYCR1 – ARCL2B ATP6V1E1 / ATP6V1A – ARCL2C ALDH18A1 – ARCL3 (De […]
https://www.cutislaxa.org/wp-content/uploads/2017/07/gene.jpg300300sonjahttp://www.cutislaxa.org/wp-content/uploads/2017/12/NEW-LOGO-CLI-4.pngsonja2017-07-01 14:38:312018-04-06 11:55:4612 different mutations have been identified
A New Type of Cutis Laxa
/in Mutations, Research, Research - Medicine - Genetics /by Marie-ClaudeIn March, the American Journal of Medecine Genetics published an article showing that a mutation on the gene PTDSS1 leads to a very rare type of Cutis Laxa : Lenz-Majewski Syndrome (LMS) . It includes Cutis Laxa with growth delay, dwarfism and intellectual delay. According to this study of 3 cases, this is a new type of […]
12 different mutations have been identified
/in Mutations /by sonjaAs of today, 12 different mutations have been identified leading to Cutis Laxa. That is why Cutis Laxa classification will soon be reviewed. Elastine (ELN) (2 mutations) – ADCL Fibuline5 (FBLN5) – ARCL1A Fibuline4 (FBLN4) – ARCL1B LTBP4 – ARCL1C ATP6V0A2 – ARCL2A PYCR1 – ARCL2B ATP6V1E1 / ATP6V1A – ARCL2C ALDH18A1 – ARCL3 (De […]