2021
DOI: 10.18233/apm42no3pp142-1482176
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Seguimiento médico de los niños con síndrome de Down

Abstract: La identificación de la alteración en el cromosoma 21 ha permitido catalogar las principales comorbilidades coexistentes en las personas con síndrome de Down. Desde 1866 John Langdon Down realizó una descripción de algunos problemas médicos en las personas con trisomía 21, pero no fue sino hasta 1970 cuando Coleman efectuó una revisión de las comorbilidades y estudios de laboratorio y gabinete que regularmente deben practicarse en esta población.

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Cited by 4 publications
(5 citation statements)
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“…There is a lack of conclusive evidence regarding the influence of cardiovascular risk factors on the incidence of cardiovascular events in DS individuals. Current health guidelines for DS mainly emphasise BMI monitoring and obesity prevention through educational efforts; however, the recommendation for periodic monitoring of the lipid profile is not indicated (Lizama et al 2013;Flores et al 2021;Michael & Marder 2021;Bull et al 2022;Dalrymple et al 2022). Furthermore, despite the recently development of guidelines aimed to the adult DS population (Tsou et al, 2020), which had been previously focused to a greater extent on paediatric population, strong recommendations for the assessment and monitoring of serum lipid levels remain unclear given the scarcity of robust evidence needed to support them.…”
Section: Discussionmentioning
confidence: 99%
“…There is a lack of conclusive evidence regarding the influence of cardiovascular risk factors on the incidence of cardiovascular events in DS individuals. Current health guidelines for DS mainly emphasise BMI monitoring and obesity prevention through educational efforts; however, the recommendation for periodic monitoring of the lipid profile is not indicated (Lizama et al 2013;Flores et al 2021;Michael & Marder 2021;Bull et al 2022;Dalrymple et al 2022). Furthermore, despite the recently development of guidelines aimed to the adult DS population (Tsou et al, 2020), which had been previously focused to a greater extent on paediatric population, strong recommendations for the assessment and monitoring of serum lipid levels remain unclear given the scarcity of robust evidence needed to support them.…”
Section: Discussionmentioning
confidence: 99%
“…11,27,46 Future directions include creating a standard workflow to screen, diagnose, and treat oSDB in patients with TS, similar to well-established clinical care guidelines for other syndromes, such as Trisomy 21 and PWS. 15,47…”
Section: Discussionmentioning
confidence: 99%
“…Clinicians should have a low threshold to refer to pediatric otolaryngology and obtain a PSG for girls with TS who have oSDB symptoms and pre‐existing conditions that have been previously linked to worsen and/or contribute to oSDB 11,27,46 . Future directions include creating a standard workflow to screen, diagnose, and treat oSDB in patients with TS, similar to well‐established clinical care guidelines for other syndromes, such as Trisomy 21 and PWS 15,47 …”
Section: Discussionmentioning
confidence: 99%
“…Children with T21 are at a higher risk of developing OSA compared to the general population, with a prevalence of 40%-80%, compared to the 1%-4% prevalence rate in healthy children. 3,16,26 In fact, all children with T21 are recommended to undergo polysomnography screening for OSA as per the American Academy of Pediatrics, 27 as even asymptomatic children have evidence of sleep apnea when tested with polysomnography. 3,5 With such high prevalence of OSA, many children with T21 undergo adenotonsillectomy as the first-line treatment for their OSA.…”
Section: Discussionmentioning
confidence: 99%