Management of Prader-Willi Syndrome 2022
DOI: 10.1007/978-3-030-98171-6_2
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Molecular Genetic Findings in Prader-Willi Syndrome

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Cited by 1 publication
(4 citation statements)
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“…Ethical difficulties, established methodology, the requirement for sufficient dosage, and long-term safety evaluations are just a few of the hurdles the sector must face. To traverse these hurdles and progress umbilical cord stem cell treatment as a possible breakthrough in the management of Prader-Willi Syndrome, researchers, medical experts, and regulatory agencies will need to work together indefinitely (Stamm, et , al , 2022).…”
Section: Discussionmentioning
confidence: 99%
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“…Ethical difficulties, established methodology, the requirement for sufficient dosage, and long-term safety evaluations are just a few of the hurdles the sector must face. To traverse these hurdles and progress umbilical cord stem cell treatment as a possible breakthrough in the management of Prader-Willi Syndrome, researchers, medical experts, and regulatory agencies will need to work together indefinitely (Stamm, et , al , 2022).…”
Section: Discussionmentioning
confidence: 99%
“…Stem cell therapy will need to be studied further and used with caution in order to reach its full potential and usher in a new age of treatment for these challenging and complex disorders. The pursuit of improvements in stem cell treatment is a critical first step in satisfying the unmet needs of persons suffering from the complex disorders Prader-Willi Syndrome (PWS) and Autism Spectrum Disorder (ASD) (Stamm, et , al , 2022). Preliminary and current research into umbilical cord stem cell treatment for PWS shows some potential for a more comprehensive therapeutic approach.…”
Section: Discussionmentioning
confidence: 99%
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