LEADER 02159nam 22005053 450 001 9910158562603321 005 20231110225924.0 010 $a9782336382302 010 $a233638230X 010 $a9782336732411 010 $a2336732416 035 $a(CKB)3810000000042281 035 $a(MiAaPQ)EBC6668580 035 $a(Au-PeEL)EBL6668580 035 $a(OCoLC)1159414730 035 $a(Exl-AI)6668580 035 $a(EXLCZ)993810000000042281 100 $a20210901d2015 uy 0 101 0 $afre 135 $aurcnu|||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aLe Syndrome D'Angelman $eParcours de Vie des Adultes 210 1$aParis :$cEditions L'Harmattan,$d2015. 210 4$dİ2015. 215 $a1 online resource (264 pages) 225 1 $aSciences et Socie?te? 311 08$a9782343057682 311 08$a2343057680 330 $aThis book, authored by Anne Chateau and Odile Piquerez, delves into the lives of adults living with Angelman Syndrome, a rare genetic disorder first described in 1965 and later confirmed in 1987. The authors draw on personal experiences and testimonies from other parents to shed light on the challenges and unique personalities of those affected by this condition. The book aims to raise awareness and understanding of the syndrome, highlighting issues such as epilepsy, motor problems, and mental and language deficits. It also explores the societal challenges and the need for inclusive practices. The intended audience includes parents, caregivers, medical professionals, and anyone interested in genetic disorders and disability advocacy.$7Generated by AI. 410 0$aSciences et Socie?te? 606 $aAngelman syndrome$7Generated by AI 606 $aGenetic disorders$7Generated by AI 615 0$aAngelman syndrome 615 0$aGenetic disorders 700 $aPiquerez$b Odile$0989406 701 $aCHATEAU$b Anne$0989407 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910158562603321 996 $aLe Syndrome D'Angelman$92262870 997 $aUNINA