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1.
Am J Med Genet A ; 194(9): e63646, 2024 09.
Artículo en Inglés | MEDLINE | ID: mdl-38702915

RESUMEN

Molecular genetics enables more precise diagnoses of skeletal dysplasia and other skeletal disorders (SDs). We investigated the clinical utility of multigene panel testing for 5011 unrelated individuals with SD in the United States (December 2019-April 2022). Median (range) age was 8 (0-90) years, 70.5% had short stature and/or disproportionate growth, 27.4% had a positive molecular diagnosis (MDx), and 30 individuals received two MDx. Genes most commonly contributing to MDx were FGFR3 (16.9%), ALPL (13.0%), and COL1A1 (10.3%). Most of the 112 genes associated with ≥1 MDx were primarily involved in signal transduction (n = 35), metabolism (n = 23), or extracellular matrix organization (n = 17). There were implications associated with specific care/treatment options for 84.4% (1158/1372) of MDx-positive individuals; >50% were linked to conditions with targeted therapy approved or in clinical development, including osteogenesis imperfecta, achondroplasia, hypophosphatasia, and mucopolysaccharidosis. Forty individuals with initially inconclusive results became MDx-positive following family testing. Follow-up mucopolysaccharidosis enzyme activity testing was positive in 14 individuals (10 of these were not MDx-positive). Our findings showed that inclusion of metabolic genes associated with SD increased the clinical utility of a gene panel and confirmed that integrated use of comprehensive gene panel testing with orthogonal testing reduced the burden of inconclusive results.


Asunto(s)
Pruebas Genéticas , Humanos , Niño , Preescolar , Adolescente , Masculino , Femenino , Lactante , Adulto , Recién Nacido , Pruebas Genéticas/métodos , Persona de Mediana Edad , Adulto Joven , Anciano , Anciano de 80 o más Años , Enfermedades del Desarrollo Óseo/genética , Enfermedades del Desarrollo Óseo/diagnóstico , Receptor Tipo 3 de Factor de Crecimiento de Fibroblastos/genética , Osteogénesis Imperfecta/genética , Osteogénesis Imperfecta/diagnóstico , Osteogénesis Imperfecta/patología , Estudios de Cohortes
2.
Biosens Bioelectron ; 261: 116432, 2024 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-38861810

RESUMEN

Haptic technology permeates diverse fields and is receiving renewed attention for VR and AR applications. Advances in flexible electronics, facilitate the integration of haptic technologies into soft wearable systems, however, because of small footprint requirements face challenges of operational time requiring either large batteries, wired connections or frequent recharge, restricting the utility of haptic devices to short-duration tasks or low duty cycles, prohibiting continuously assisting applications. Currently many chronic applications are not investigated because of this technological gap. Here, we address wireless power and operation challenges with a biosymbiotic approach enabling continuous operation without user intervention, facilitated by wireless power transfer, eliminating the need for large batteries, and offering long-term haptic feedback without adhesive attachment to the body. These capabilities enable haptic feedback for robotic surgery training and posture correction over weeks of use with neural net computation. The demonstrations showcase that this device class expands use beyond conventional brick and strap or epidermally attached devices enabling new fields of use for imperceptible therapeutic and assistive haptic technologies supporting care and disease management.


Asunto(s)
Técnicas Biosensibles , Diseño de Equipo , Dispositivos Electrónicos Vestibles , Humanos , Técnicas Biosensibles/instrumentación , Tacto , Interfaz Usuario-Computador , Retroalimentación Sensorial , Tecnología Inalámbrica , Procedimientos Quirúrgicos Robotizados/instrumentación , Robótica/instrumentación
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