Intellectual Disability and Solid Organ Transplantations

Sözlük T. Türk Dil Kurumu | Sözlük [Internet]. Sozluk.gov.tr. 2022 [cited 7 April 2022]. Available from: https://sozluk.gov.tr/

American Psychiatric Association. The Diagnostic and Statistical Manual of Mental Disorders. Fifth Edit. 2013

Akın Sarı B, Baskın S, Özçay F, Sezgin A, Haberal M. Psychiatric Evaluation of Children During the Organ Transplant Process. Experimental and Clinical Transplantation. 2018;.

Wightman A, Bradford M, Hsu E, Bartlett H, Smith J. Prevalence and Long-Term Outcomes of Solid Organ Transplant in Children with Intellectual Disability. The Journal of Pediatrics. 2021;235:10-17.e4.

Souza L, Santos A, Sgardioli I, Viguetti‐Campos N, Marques Prota J, Oliveira‐Sobrinho R et al. Phenotype comparison among individuals with developmental delay/intellectual disability with or without genomic imbalances. Journal of Intellectual Disability Research. 2019;63(11):1379-1389.

Baldwin N, Gray M, Patel C, Al Diffalha S. Acute Liver Failure Due to Toxoplasmosis After Orthotopic Liver Transplantation. Journal of Investigative Medicine High Impact Case Reports. 2021;9:232470962110146.

Anlar B, Erman H. Zihinsel Gelişim (Zeka) Gerilikleri. In: Çuhadaroğlu Çetin F, Coşkun A, İşeri E, Miral S, Motavallı N, Pehlivantürk B, Türkbay T, Uslu R, Ünal F eds. Çocuk ve Ergen Psikiyatrisi Temel Kitabı. Ankara: Hekimler Yayın Birliği;2008. p: 187-199.

Bartter Syndrome - NORD (National Organization for Rare Disorders) [Internet]. NORD (National Organization for Rare Disorders). 2022 [cited 7 April 2022]. Available from: https://rarediseases.org/rare-diseases/bartters-syndrome/

Rodriguez JD, Bhat SS, Meloni I, Ladd S, Leslie ND, Doyne EO, et al. Intellectual disability, midface hypoplasia, facial hypotonia, and alport syndrome are associated with a deletion in Xq22.3. American Journal of Medical Genetics Part A. 2010 Mar;152A(3):713–7.

Casey JP, Slattery S, Cotter M, Monavari AA, Knerr I, Hughes J, et al. Clinical and genetic characterisation of infantile liver failure syndrome type 1, due to recessive mutations in LARS. Journal of Inherited Metabolic Disease [Internet]. 2015 Nov 1 [cited 2021 Apr 3];38(6):1085–92. Available from: https://pubmed.ncbi.nlm.nih.gov/25917789/

Van Maldergem L. Berardinelli-Seip Congenital Lipodystrophy. 2003 Sep 8 [Updated 2016 Dec 8]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2021. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1212/

Barakat AJ, Raygada M, Rennert OM. Barakat syndrome revisited. American Journal of Medical Genetics Part A [Internet]. 2018 Apr 16 [cited 2021 Oct 7];176(6):1341–8. Available from: https://www.thelancet.com/action/showPdf?pii=S0140-6736%2818%2931178-4

Afshar S, Porter M, Barton B, Stormon M. Intellectual and academic outcomes after pediatric liver transplantation: Relationship with transplant-related factors. American Journal of Transplantation. 2018 Jun 16;18(9):2229–37.

Hoytema van Konijnenburg EMM, Wortmann SB, Koelewijn MJ, Tseng LA, Houben R, Stöckler-Ipsiroglu S, et al. Treatable inherited metabolic disorders causing intellectual disability: 2021 review and digital app. Orphanet Journal of Rare Diseases. 2021 Apr 12;16(1).

Shriver TP. The discriminatory reason doctors won’t give a baby the heart she needs. Washington Post [Internet]. 2016 Apr 8 [cited 2022 Apr 7]; Available from: https://www.Washingtonpost.com/opinions/this-is-the-reason-doctors-wont-give-a-baby-the-heart-she-needs/2016/04/08/d766816c-fcea-11e5-886f-a037dba38301_story.html?utm_term=.6742500eec2d.

Goel AN, Iyengar A, Schowengerdt K, Fiore AC, Huddleston CB. Heart transplantation in children with intellectual disability: An analysis of the UNOS database. Pediatric Transplantation 2017;21:e12858 doi:10.1111/petr.12585

Sözlük T. Türk Dil Kurumu | Sözlük [Internet]. Sozluk.gov.tr. 2022 [cited 7 April 2022]. Available from: https://sozluk.gov.tr/

American Psychiatric Association. The Diagnostic and Statistical Manual of Mental Disorders. Fifth Edit. 2013

Akın Sarı B, Baskın S, Özçay F, Sezgin A, Haberal M. Psychiatric Evaluation of Children During the Organ Transplant Process. Experimental and Clinical Transplantation. 2018;.

Wightman A, Bradford M, Hsu E, Bartlett H, Smith J. Prevalence and Long-Term Outcomes of Solid Organ Transplant in Children with Intellectual Disability. The Journal of Pediatrics. 2021;235:10-17.e4.

Souza L, Santos A, Sgardioli I, Viguetti‐Campos N, Marques Prota J, Oliveira‐Sobrinho R et al. Phenotype comparison among individuals with developmental delay/intellectual disability with or without genomic imbalances. Journal of Intellectual Disability Research. 2019;63(11):1379-1389.

Baldwin N, Gray M, Patel C, Al Diffalha S. Acute Liver Failure Due to Toxoplasmosis After Orthotopic Liver Transplantation. Journal of Investigative Medicine High Impact Case Reports. 2021;9:232470962110146.

Anlar B, Erman H. Zihinsel Gelişim (Zeka) Gerilikleri. In: Çuhadaroğlu Çetin F, Coşkun A, İşeri E, Miral S, Motavallı N, Pehlivantürk B, Türkbay T, Uslu R, Ünal F eds. Çocuk ve Ergen Psikiyatrisi Temel Kitabı. Ankara: Hekimler Yayın Birliği;2008. p: 187-199.

Bartter Syndrome - NORD (National Organization for Rare Disorders) [Internet]. NORD (National Organization for Rare Disorders). 2022 [cited 7 April 2022]. Available from: https://rarediseases.org/rare-diseases/bartters-syndrome/

Rodriguez JD, Bhat SS, Meloni I, Ladd S, Leslie ND, Doyne EO, et al. Intellectual disability, midface hypoplasia, facial hypotonia, and alport syndrome are associated with a deletion in Xq22.3. American Journal of Medical Genetics Part A. 2010 Mar;152A(3):713–7.

Casey JP, Slattery S, Cotter M, Monavari AA, Knerr I, Hughes J, et al. Clinical and genetic characterisation of infantile liver failure syndrome type 1, due to recessive mutations in LARS. Journal of Inherited Metabolic Disease [Internet]. 2015 Nov 1 [cited 2021 Apr 3];38(6):1085–92. Available from: https://pubmed.ncbi.nlm.nih.gov/25917789/

Van Maldergem L. Berardinelli-Seip Congenital Lipodystrophy. 2003 Sep 8 [Updated 2016 Dec 8]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2021. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1212/

Barakat AJ, Raygada M, Rennert OM. Barakat syndrome revisited. American Journal of Medical Genetics Part A [Internet]. 2018 Apr 16 [cited 2021 Oct 7];176(6):1341–8. Available from: https://www.thelancet.com/action/showPdf?pii=S0140-6736%2818%2931178-4

Afshar S, Porter M, Barton B, Stormon M. Intellectual and academic outcomes after pediatric liver transplantation: Relationship with transplant-related factors. American Journal of Transplantation. 2018 Jun 16;18(9):2229–37.

Hoytema van Konijnenburg EMM, Wortmann SB, Koelewijn MJ, Tseng LA, Houben R, Stöckler-Ipsiroglu S, et al. Treatable inherited metabolic disorders causing intellectual disability: 2021 review and digital app. Orphanet Journal of Rare Diseases. 2021 Apr 12;16(1).

Shriver TP. The discriminatory reason doctors won’t give a baby the heart she needs. Washington Post [Internet]. 2016 Apr 8 [cited 2022 Apr 7]; Available from: https://www.Washingtonpost.com/opinions/this-is-the-reason-doctors-wont-give-a-baby-the-heart-she-needs/2016/04/08/d766816c-fcea-11e5-886f-a037dba38301_story.html?utm_term=.6742500eec2d.

Goel AN, Iyengar A, Schowengerdt K, Fiore AC, Huddleston CB. Heart transplantation in children with intellectual disability: An analysis of the UNOS database. Pediatric Transplantation 2017;21:e12858 doi:10.1111/petr.12585