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1.
Genes (Basel) ; 14(9)2023 08 23.
Artículo en Inglés | MEDLINE | ID: mdl-37761804

RESUMEN

Snijders Blok-Campeau syndrome (SNIBCPS, OMIM# 618205) is an extremely infrequent disease with only approximately 60 cases reported so far. SNIBCPS belongs to the group of neurodevelopmental disorders (NDDs). Clinical features of patients with SNIBCPS include global developmental delay, intellectual disability, speech and language difficulties and behavioral disorders like autism spectrum disorder. In addition, patients with SNIBCPS exhibit typical dysmorphic features including macrocephaly, hypertelorism, sparse eyebrows, broad forehead, prominent nose and pointed chin. The severity of the neurological effects as well as the presence of other features is variable among subjects. SNIBCPS is caused likely by pathogenic and pathogenic variants in CHD3 (Chromodomain Helicase DNA Binding Protein 3), which seems to be involved in chromatin remodeling by deacetylating histones. Here, we report 20 additional patients with clinical features compatible with SNIBCPS from 17 unrelated families with confirmed likely pathogenic/pathogenic variants in CHD3. Patients were analyzed by whole exome sequencing and segregation studies were performed by Sanger sequencing. Patients in this study showed different pathogenic variants affecting several functional domains of the protein. Additionally, none of the variants described here were reported in control population databases, and most computational predictors suggest that they are deleterious. The most common clinical features of the whole cohort of patients are global developmental delay (98%) and speech disorder/delay (92%). Other frequent features (51-74%) include intellectual disability, hypotonia, hypertelorism, abnormality of vision, macrocephaly and prominent forehead, among others. This study expands the number of individuals with confirmed SNIBCPS due to pathogenic or likely pathogenic variants in CHD3. Furthermore, we add evidence of the importance of the application of massive parallel sequencing for NDD patients for whom the clinical diagnosis might be challenging and where deep phenotyping is extremely useful to accurately manage and follow up the patients.


Asunto(s)
Discapacidades del Desarrollo , Hipertelorismo , Discapacidad Intelectual , Trastornos del Desarrollo del Lenguaje , Megalencefalia , Humanos , ADN Helicasas/genética , Histonas , Discapacidad Intelectual/genética , Megalencefalia/genética , Complejo Desacetilasa y Remodelación del Nucleosoma Mi-2/genética , Discapacidades del Desarrollo/genética
3.
Health Informatics J ; 22(4): 975-983, 2016 12.
Artículo en Inglés | MEDLINE | ID: mdl-26351262

RESUMEN

The incorporation of an electronic medical record into patient care is a priority in developed countries, but faces significant obstacles for adoption in developing countries. The goal of our study was to define and assess the efficiency of a personalized intervention on village physicians' use of electronic medical records in rural community health services of underprivileged areas. Six towns were selected with two bordering local health stations from each town. One was randomly given to the intervention group and the other to the control group. A structured on-site intervention was provided to village physicians in the intervention group, for 7 months. The results showed that in the intervention group, the percentage of households with complete records increased. The percentage of clinic medical records and complete child vaccination in the intervention group also increased from 2 to 14 percent (p = <0.05) and from 10 to 23 percent (p = 0.05), respectively. Our investigation demonstrated that on-site education, supervision, and technical support directly correlate with improved use of electronic medical record. Our results report the challenges in implementing such a system and the steps being taken to enhance likelihood of sustainability.


Asunto(s)
Países en Desarrollo/estadística & datos numéricos , Registros Electrónicos de Salud/estadística & datos numéricos , Desarrollo de Programa/métodos , Adolescente , Adulto , Anciano , Niño , República Dominicana , Registros Electrónicos de Salud/normas , Femenino , Humanos , Masculino , Persona de Mediana Edad , Aceptación de la Atención de Salud , Encuestas y Cuestionarios
4.
Lima; s.n; 1986. 54 p. ilus, tab. (T-3253).
Monografía en Español | LILACS | ID: lil-186957

RESUMEN

Por su contenido en calcio, fósforo, fierro, el producto fresco del "apio", tiene un poder mineralizante apreciable, constituyendo también una fuente de vitaminas. El apio liofilizado es altamente higroscópico debido a su elevada parasidad y bajo contenido de humedad residual. El apio liofilizado en la evaluación organoléptica tiene un alto grado de aceptabilidad casi similar al producto fresco. Mediante los resultados obtenidos, la temperatura óptima de rehidratación es de 100ºC, alcanzando un 89 por ciento, en el producto liofilizado, produciendo una menor rehidratación a 60ºC y 20ºC respectivamente. La liofilización es un sistema eficaz para observar la sobreproducción agrícolas, permitiendo una reducción de peso, haciendo el costo de transporte más económico alargando a su vez el período de vida, siempre que estén protegidos convenientemente.


Asunto(s)
Apium , Calidad de los Alimentos , Liofilización
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