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1.
Pediatr Dermatol ; 41(2): 270-274, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-38239057

RESUMEN

The rate of pediatric hospitalization for cutaneous pathology has been increasing in recent years, often requiring the expertise of consulting pediatric dermatologists; however, the infrastructure of inpatient pediatric dermatology consultative services remains poorly characterized. We sought to assess the structure, consult volume, physician compensation, and utilization of teledermatology in pediatric dermatology inpatient services to better understand the current care model. Our survey of 118 pediatric dermatologists revealed that 89% of respondents see between 1 and 10 new consults per week, 39% perform all inpatient consults including evening and weekends without assistance from other providers, 71% do not have protected time during the week to provide inpatient consultations, and only 10% receive financial compensation via stipend. By highlighting both the high demand for pediatric consultative dermatology as well as the significant burden placed on these providers by existing practice models, we hope to encourage a reappraisal of the current infrastructure of pediatric inpatient dermatology to increase structural and financial support for this vital service.


Asunto(s)
Dermatología , Humanos , Niño , Estados Unidos , Piel , Encuestas y Cuestionarios , Recursos Humanos , Derivación y Consulta
2.
Pediatr Dermatol ; 38(6): 1590-1591, 2021 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-34725860

RESUMEN

RAS-related C3 Botulinum Toxin Substrate 1 (RAC1) is a Rho GTPase that modulates numerous cellular functions including transcriptional regulation and actin-based structure turnover. Reported de novo RAC1 mutations are rare but generally manifest in developmental delay and brain malformations. In Rac1 knockout mice, a hairless phenotype has been observed, but little is known of other cutaneous phenotypes of RAC1 mutations. In this report, we describe the first known case of a RAC1 mutation with ichthyosiform changes.


Asunto(s)
Ictiosis/genética , Proteína de Unión al GTP rac1 , Animales , Humanos , Ratones , Mutación , Proteína de Unión al GTP rac1/genética
3.
Proc (Bayl Univ Med Cent) ; 34(3): 409-411, 2021 Jan 11.
Artículo en Inglés | MEDLINE | ID: mdl-33953481

RESUMEN

Kawasaki disease is a vasculitis of medium-sized vessels and the most common cause of acquired heart defects in the United States. Although its etiology is unclear, an infectious trigger has been theorized, which has been highlighted by the recent pandemic. We present a case of a 17-month-old-girl with concurrent Kawasaki disease and non-SARS-CoV2 coronavirus infection and a sequela of onychomadesis.

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