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How can clinical ethics guide the management of comorbidities in the child with Rett syndrome?

Rett syndrome is a rare disorder caused by a mutation in the MECP2 gene. Those affected generally have severe functional impairments and medical comorbidities such as scoliosis and poor growth are common. There is a paucity of information on the natural history of many rare disorders and an even gre...

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Bibliografske podrobnosti
izdano v:J Paediatr Child Health
Main Authors: Downs, Jenny, Forbes, David, Johnson, Michael, Leonard, Helen
Format: Artigo
Jezik:Inglês
Izdano: 2016
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4990489/
https://ncbi.nlm.nih.gov/pubmed/27243819
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jpc.13241
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