Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 72
Filtrar
Más filtros

Banco de datos
País/Región como asunto
Tipo del documento
Intervalo de año de publicación
1.
Pediatr Dermatol ; 2024 Jul 25.
Artículo en Inglés | MEDLINE | ID: mdl-39054583

RESUMEN

Sepsis is a leading cause of death in preterm neonates. The increased susceptibility to sepsis is due to prolonged hospitalization, the need for invasive procedures, and immaturity of innate and adaptive immunity. Chlorhexidine gluconate is a popular topical disinfectant that was not recommended for use in preterm neonates until 2012. Thus, there are few studies assessing the role of chlorhexidine gluconate in antisepsis for preterm neonates. A better understanding of the safety and efficacy of chlorhexidine gluconate as an antiseptic agent for preterm neonates is the first step in establishing best practice guidelines for this population.

2.
Dermatol Surg ; 49(1): 25-28, 2023 01 01.
Artículo en Inglés | MEDLINE | ID: mdl-36533791

RESUMEN

BACKGROUND: The h-index is a measure of research achievement using not only the number of publications of an individual, but also the impact of the publications. OBJECTIVE: The objective of this study is to evaluate the h-indices of Mohs surgeons within a variety of practice settings. MATERIALS AND METHODS: A list of all American College of Mohs Society (ACMS) members with corresponding fellowships years were collected using the ACMS membership directory. Publicly available demographic information was obtained including fellowship year, practice setting, PhD status, practice location (region), total number of publications, and h-index. Descriptive statistics were calculated to compare h-indices among the demographic data. RESULTS: A total of 1150 ACMS members were included. The Practice setting distribution was as follows: 10.6% academic, 85.7% private practice, and 3.7% combined. H-index differed significantly based on practice setting (p < .001), with higher h-indices in academic and combined settings compared with the private practice setting. Subanalysis among academic Mohs surgeons revealed higher mean h-indices among professors (23.9) > associate professors (10.6) > assistant professors (8.6) > clinical instructors (5) (p < .001). CONCLUSION: H-indices were highest among Mohs surgeons in the academic setting with increasing values correlating with higher academic rank and time since fellowship completion.


Asunto(s)
Éxito Académico , Cirujanos , Humanos , Estados Unidos , Becas , Eficiencia
3.
Pediatr Dermatol ; 40(4): 688-690, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-36623811

RESUMEN

A female twin presented at birth with a collodion membrane on the hands and feet. After the membrane resolved over the first months of life, she was initially diagnosed with acral self-healing collodion membrane. However, she subsequently developed brown well-defined geometric scales on the trunk and extremities, consistent with ichthyosis. Genetic testing showed a heterozygous pathogenic variant in ELOVL4, a gene associated with syndromic ichthyosis with developmental delay, seizures, and spasticity. Although acral collodion membrane is considered to be a benign variant of the more generalized collodion, usually described as "self-healing," it may be the initial presentation of more diffuse ichthyosis.


Asunto(s)
Ictiosis Lamelar , Ictiosis , Recién Nacido , Humanos , Femenino , Colodión , Ictiosis Lamelar/diagnóstico , Ictiosis Lamelar/genética , Ictiosis/genética , Heterocigoto , Mano/patología , Proteínas del Ojo/genética , Proteínas de la Membrana/genética
4.
Pediatr Dermatol ; 40(6): 1086-1090, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-37002583

RESUMEN

Pyoderma gangrenosum is a rare neutrophilic dermatosis characterized by painful skin ulcers with necrotic, undermined margins. In severe cases, particularly in pediatric patients, work-up for an associated autoimmune, inflammatory, malignant, or genetic disorder should be considered based on the clinical presentation. We report a unique case of pediatric pyoderma gangrenosum with a leukemoid reaction, secondary to an autosomal recessive leukocyte adhesion deficiency type 1.


Asunto(s)
Reacción Leucemoide , Síndrome de Deficiencia de Adhesión del Leucocito , Piodermia Gangrenosa , Úlcera Cutánea , Humanos , Niño , Piodermia Gangrenosa/complicaciones , Piodermia Gangrenosa/diagnóstico , Síndrome de Deficiencia de Adhesión del Leucocito/complicaciones , Síndrome de Deficiencia de Adhesión del Leucocito/diagnóstico , Síndrome de Deficiencia de Adhesión del Leucocito/genética , Reacción Leucemoide/complicaciones
5.
Pediatr Dermatol ; 40(1): 129-131, 2023 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-36385397

RESUMEN

Despite advances in our understanding of the human microbiome, there exist significant knowledge gaps in our understanding of the skin microbiome of the preterm neonate. Herein, we describe skin microbiome sampling of six preterm neonates at multiple timepoints, and compare the skin microbiome samples to environmental (crib/isolette swabs) and negative controls. Samples of the same type (skin, crib, control) were more similar than when compared by week or by patient.


Asunto(s)
Recien Nacido Prematuro , Microbiota , Recién Nacido , Humanos , Piel
6.
Pediatr Dermatol ; 39(1): 151-152, 2022 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-34787337

RESUMEN

Congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome is a rare X-linked dominant disorder of cholesterol synthesis characterized by unilateral ichthyosiform dermatitis with ipsilateral limb hypoplasia. Recently, pathogenesis-based treatment has demonstrated improvement of skin lesions with statins by decreasing formation of cholesterol intermediates through inhibition of cholesterol synthesis. We report a 10-month-old girl who presented with unilateral scaly ptychotropic plaques, who experienced rapid, near-complete clearance with topical 5% simvastatin monotherapy twice daily.


Asunto(s)
Eritrodermia Ictiosiforme Congénita , Deformidades Congénitas de las Extremidades , Anomalías Múltiples , Femenino , Enfermedades Genéticas Ligadas al Cromosoma X , Humanos , Eritrodermia Ictiosiforme Congénita/tratamiento farmacológico , Lactante , Pomadas , Simvastatina/uso terapéutico
7.
Pediatr Dermatol ; 38(1): 83-87, 2021 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-33063877

RESUMEN

BACKGROUND/OBJECTIVES: Premature infants have lower rates of atopic dermatitis (AD) compared with full-term infants, though little is known about the factors contributing to this association. We explored the infant and environmental factors that may contribute to the association between prematurity and atopic dermatitis, including mode of delivery, birthweight, gestation, and duration of stay in the neonatal intensive care unit (NICU). METHODS: This was a single-center retrospective study. Independent samples t tests or chi-square tests were used to compare groups on continuous and categorical variables, respectively. Logistic regression then examined the association of the predictor variables with AD. RESULTS: Four thousand sixteen mother-infant dyads were included. Infants had a higher risk of developing AD if they were delivered vaginally (P = .013), did not stay in the NICU (P < .001), had a longer gestation (P = .001), or had a higher birthweight (P = .002). In modeling atopic dermatitis with the predictor variables, only NICU length of stay remained significantly associated with a lower risk of AD (P = .004). CONCLUSION: Infants had a lower risk of developing AD if they had a longer stay in the NICU.


Asunto(s)
Dermatitis Atópica , Unidades de Cuidado Intensivo Neonatal , Dermatitis Atópica/epidemiología , Femenino , Humanos , Lactante , Recién Nacido , Recien Nacido Prematuro , Tiempo de Internación , Estudios Retrospectivos
8.
Pediatr Dermatol ; 38(4): 879-882, 2021 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-34227145

RESUMEN

A 7-year-old girl with a history of Langerhans cell histiocytosis (LCH), in remission, presented with the sudden appearance of multiple, agminated nevi. Skin biopsy revealed a benign junctional nevus, without recurrence of LCH. Subsequent immunohistochemical testing of both the skin and iliac wing biopsies demonstrated a BRAF V600E mutation. MAPK pathway mutations have been implicated in both LCH and nevogenesis.


Asunto(s)
Histiocitosis de Células de Langerhans , Nevo Pigmentado , Nevo , Neoplasias Cutáneas , Niño , Femenino , Histiocitosis de Células de Langerhans/complicaciones , Histiocitosis de Células de Langerhans/diagnóstico , Humanos , Mutación , Recurrencia Local de Neoplasia , Proteínas Proto-Oncogénicas B-raf/genética
9.
Pediatr Dermatol ; 38(1): 249-252, 2021 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-33222239

RESUMEN

The initial clinical presentation of infantile myofibromatosis can vary from subtle skin changes to large tumors. Here, we describe a case of congenital generalized infantile myofibromatosis which presented with diffuse hypopigmented macules, some with subtle atrophy and telangiectasia. Further workup revealed visceral involvement which led to treatment with systemic chemotherapy. Awareness of this rare clinical presentation is crucial to expedite workup and treatment given the poor prognosis in infants with visceral involvement.


Asunto(s)
Miofibromatosis , Humanos , Lactante , Recién Nacido , Miofibromatosis/diagnóstico
10.
Dermatol Ther ; 33(1): e13202, 2020 01.
Artículo en Inglés | MEDLINE | ID: mdl-31858672

RESUMEN

Androgenetic alopecia (AGA) is common and associated with significant psychosocial distress. Treatment options are needed for patients that do not adequately respond to first line treatments of finasteride or minoxidil. Topical ketoconazole has been proposed as a promising treatment. The goal of this systematic review was to evaluate the efficacy of topical ketoconazole in the treatment of AGA. A systematic literature search was conducted within the MEDLINE database using the key terms "ketoconazole" and "alopecia." Forty-seven papers were screened for inclusion, of which nine were assessed for eligibility. Seven articles were included in the qualitative synthesis, including two animal studies (total of 40 participants) and five human studies (total of 318 participants). Murine studies demonstrated a significant increase in mean ratio of hair regrowth to denuded area in the ketoconazole treatment groups compared to controls. Human studies reported increased hair shaft diameter following ketoconazole use. One study reported a significant increase in pilary index (percent anagen phase × diameter) following treatment. Studies also demonstrated clinical improvement of AGA based on photographic assessment and subjective evaluation. Topical ketoconazole is a promising adjunctive or alternative therapy in the treatment of AGA. Randomized controlled trials are needed.


Asunto(s)
Alopecia/tratamiento farmacológico , Cabello/crecimiento & desarrollo , Cetoconazol/administración & dosificación , Administración Tópica , Animales , Humanos , Ratones , Resultado del Tratamiento
11.
Dermatol Ther ; 33(6): e14386, 2020 11.
Artículo en Inglés | MEDLINE | ID: mdl-33044025

RESUMEN

Molluscum contagiosum (MC) is a common cutaneous viral infection with no standard treatment. The virus responsible for MC is thought to be cleared by cell mediated immunity (CMI). Intralesional immunotherapy that stimulates CMI has been shown to be an effective treatment for other cutaneous viruses. In this review, we evaluate the efficacy and safety of intralesional immunotherapy in the treatment of MC. Articles met inclusion criteria if they examined the effects of intralesional immunotherapy as a treatment for MC, with a clear outcome and reproducible methodology. 228 studies were screened and 10 studies met criteria for inclusion. Intralesional immunotherapies investigated included candida, combined measles, mumps, rubella vaccine, tuberculin purified protein derivative, vitamin D3, interferon α, and Streptococcal substrain OK-432. Studies demonstrated clearance of MC lesions following intralesional immunotherapy, with complete response rates between 36% and 100%. No serious adverse effects were noted. Intralesional immunotherapy is a safe and effective treatment option for MC in pediatric and adult patients.


Asunto(s)
Molusco Contagioso , Adulto , Niño , Humanos , Factores Inmunológicos/uso terapéutico , Inmunoterapia/efectos adversos , Inyecciones Intralesiones , Molusco Contagioso/tratamiento farmacológico , Tuberculina
12.
Pediatr Dermatol ; 37(2): 265-271, 2020 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-31930595

RESUMEN

Cutaneous warts are a common pediatric complaint with modest response to first-line treatments. Warts are a manifestation of human papillomavirus (HPV) infection and are cleared by cell-mediated immunity (CMI). Intralesional immunotherapy treatments have been studied as alternative therapies, particularly for recalcitrant or multiple warts, including Candida antigen, mumps antigen, the combined measles, mumps, and rubella (MMR) vaccine, tuberculin purified protein derivative (PPD), and bacille Calmette-Guerin (BCG) vaccine. These treatments are thought to increase HPV recognition by stimulating CMI. In this review, we evaluate and compare the efficacy and adverse effects of intralesional immunotherapy in the treatment of pediatric warts. Articles met inclusion criteria if they specifically evaluated the effects of intralesional immunotherapy (candida, MMR, tuberculin PPD, or BCG) as treatment for cutaneous warts in a pediatric population, and if they quantified treatment effect in a reproducible manner. Twenty-one studies met criteria. Many studies demonstrated complete clearance of injected common warts in pediatric patients with clearance rates ranging from 23.3% to 95.2%. Distant wart resolution was common. Intralesional immunotherapy is a promising treatment option for cutaneous warts in children.


Asunto(s)
Inmunoterapia , Verrugas/terapia , Humanos , Inyecciones Intralesiones
13.
Pediatr Dermatol ; 37(1): 217-218, 2020 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-31373408

RESUMEN

Microphthalmia and linear skin defects syndrome (MLS) is a rare X-linked dominant disorder characterized by microphthalmia and linear atrophic plaques of the face and neck. The diagnosis of MLS can be challenging secondary to both its rarity and to clinical overlap with Goltz syndrome. Whereas the skin lesions of MLS are more likely to improve in appearance with age, the lesions of Goltz are typically persistent.


Asunto(s)
Anomalías Múltiples/diagnóstico , Enfermedades Genéticas Ligadas al Cromosoma X/diagnóstico , Microftalmía/diagnóstico , Anomalías Cutáneas/diagnóstico , Diagnóstico Diferencial , Femenino , Hipoplasia Dérmica Focal/diagnóstico , Humanos , Recién Nacido , Pronóstico , Síndrome
14.
Pediatr Dermatol ; 37(6): 1094-1097, 2020 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-32892414

RESUMEN

BACKGROUND/OBJECTIVE: The h-index is a measure of research achievement. Individuals with similar h-indices should be equivalent in terms of scientific impact. However, this value is inherently biased toward fields with higher visibility and readership. To utilize the power of h-indices in predicting future research success and as a benchmark for academic advancement, niche fields like pediatric dermatology must be examined independently. METHODS: Publicly available data were examined. A list of current pediatric dermatologists were obtained from the Society for Pediatric Dermatology's member directory. The following demographic information was obtained: fellowship certification year, PhD status, prior pediatric residency training, state/region, practice setting, academic appointment, number of publications, and h-index. Descriptive and analytic statistics were calculated. RESULTS: A total of 317 pediatric dermatologists were included. Practice setting distribution was as follows: 54.3% academic, 32.5% non-academic, and 13.3% combined. H-index differed significantly based on pediatric dermatology certification year (P < .001), increasing as time from certification increased. Those in academics had higher h-indices than those in both non-academic and combined practice settings (P < .001 and .007, respectively). Professors (25.0) had higher h-indices than associate professors (11.0), who had higher h-indices than assistant professors (4.4) (P < .001). CONCLUSIONS: H-index increased with increasing academic rank and was highest among those working in academics. For pediatric dermatologists considering application for promotion, the h-index for each level can serve as a useful benchmark to guide decision-making.


Asunto(s)
Dermatólogos , Dermatología , Bibliometría , Niño , Eficiencia , Docentes Médicos , Humanos , Estados Unidos
15.
Alcohol Clin Exp Res ; 43(10): 2167-2178, 2019 10.
Artículo en Inglés | MEDLINE | ID: mdl-31386211

RESUMEN

BACKGROUND: The nociceptin/orphanin FQ opioid peptide (NOP) receptor and its endogenous ligand N/OFQ have been implicated in the regulation of drug and alcohol use disorders (AUD). In particular, evidence demonstrated that NOP receptor activation blocks reinforcing and motivating effects of alcohol across a range of behavioral measures, including alcohol intake, conditioned place preference, and vulnerability to relapse. METHODS: Here, we show the effects of pharmacological activation and inhibition of NOP receptors on binge-like alcohol consumption, as measured by the "drinking in the dark" (DID) model in C57BL/6J mice. RESULTS: We found that 2 potent and selective NOP agonists AT-202 (0, 0.3, 1, 3 mg/kg) and AT-312 (0, 0.3, 1 mg/kg) did not affect binge alcohol drinking at doses that do not affect locomotor activity. AT-202 also failed to alter DID behavior when administered to mice previously exposed to chronic alcohol treatment with an alcohol-containing liquid diet. Conversely, treatment with either the high affinity NOP receptor antagonist SB-612111 (0, 3, 10, 30 mg/kg) or the selective antagonist LY2817412 (0, 3, 10, 30 mg/kg) decreased binge drinking. SB-612111 was effective at all doses examined, and LY2817412 was effective at 30 mg/kg. Consistently, NOP receptor knockout mice consumed less alcohol compared to wild type. SB-612111 reduced DID and increased sucrose consumption at doses that do not appear to affect locomotor activity. However, the high dose of SB-612111 (30 mg/kg) reduced alcohol intake but failed to inhibit preference in a 2-bottle choice DID model that can assess moderate alcohol intake. CONCLUSIONS: The present results suggest that NOP receptor inhibition rather than activation may represent a valuable approach for treatment of AUD characterized by excessive alcohol consumption such as binge drinking.


Asunto(s)
Disuasivos de Alcohol/uso terapéutico , Consumo de Bebidas Alcohólicas/prevención & control , Antagonistas de Narcóticos/uso terapéutico , Receptores Opioides/efectos de los fármacos , Consumo de Bebidas Alcohólicas/genética , Consumo de Bebidas Alcohólicas/psicología , Animales , Consumo Excesivo de Bebidas Alcohólicas/tratamiento farmacológico , Consumo Excesivo de Bebidas Alcohólicas/genética , Consumo Excesivo de Bebidas Alcohólicas/psicología , Depresores del Sistema Nervioso Central/sangre , Cicloheptanos/farmacología , Oscuridad , Relación Dosis-Respuesta a Droga , Etanol/sangre , Indoles/farmacología , Masculino , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Actividad Motora/efectos de los fármacos , Piperidinas/farmacología , Receptores Opioides/agonistas , Receptores Opioides/genética , Receptor de Nociceptina
16.
J Am Acad Dermatol ; 80(5): 1233-1250.e10, 2019 May.
Artículo en Inglés | MEDLINE | ID: mdl-30236514

RESUMEN

Acquired hypopigmented skin changes are commonly encountered by dermatologists. Although hypopigmentation is often asymptomatic and benign, occasional serious and disabling conditions present with cutaneous hypopigmentation. A thorough history and physical examination, centered on disease distribution and morphologic findings, can aid in delineating the causes of acquired hypopigmented disorders. The second article in this 2-part continuing medical education series focuses on conditions with a hypopigmented phenotype. Early diagnosis and appropriate management of these disorders can improve a patient's quality of life, halt disease progression, and prevent irreversible disability.


Asunto(s)
Hipopigmentación/etiología , Micosis Fungoide/complicaciones , Neoplasias Cutáneas/complicaciones , Intoxicación por Arsénico/complicaciones , Dermatitis/complicaciones , Humanos , Hipopigmentación/diagnóstico , Hipopigmentación/terapia , Leishmaniasis Visceral/complicaciones , Lepra Paucibacilar/complicaciones , Micosis Fungoide/diagnóstico , Neoplasias Cutáneas/diagnóstico , Sífilis/complicaciones , Tiña Versicolor/complicaciones , Tiña Versicolor/tratamiento farmacológico
17.
J Am Acad Dermatol ; 80(5): 1215-1231.e6, 2019 May.
Artículo en Inglés | MEDLINE | ID: mdl-30236516

RESUMEN

Acquired disorders with depigmentation are commonly encountered by dermatologists and present with a wide differential diagnosis. Vitiligo, the most common disorder of acquired depigmentation, is characterized by well-defined depigmented macules and patches. Other conditions, such as chemical leukoderma, can present with similar findings, and are often easily mistaken for vitiligo. Key clinical features can help differentiate between acquired disorders of depigmentation. The first article in this continuing medical education series focuses on conditions with a vitiligo-like phenotype. Early recognition and adequate treatment of these conditions is critical in providing appropriate prognostication and treatment.


Asunto(s)
Melanoma/complicaciones , Regresión Neoplásica Espontánea , Trastornos de la Pigmentación/etiología , Neoplasias Cutáneas/complicaciones , Dermatitis/complicaciones , Humanos , Liquen Escleroso y Atrófico/complicaciones , Oncocercosis/complicaciones , Trastornos de la Pigmentación/inducido químicamente , Trastornos de la Pigmentación/patología , Pinta (Dermatosis)/complicaciones , Esclerodermia Localizada/complicaciones , Esclerodermia Sistémica/complicaciones , Síndrome Uveomeningoencefálico/complicaciones
18.
J Am Acad Dermatol ; 81(6): 1277-1282, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-30991120

RESUMEN

BACKGROUND: Klippel-Trenaunay syndrome (KTS) is a vascular malformation overgrowth syndrome characterized by capillary malformation, venous malformation, and limb overgrowth, with or without lymphatic malformation. Patients are at an increased risk of hemorrhage and venous thromboembolism (VTE). Consequently, women with this condition often are counseled to avoid pregnancy, but minimal data are available on the relationship between pregnancy, VTE, and bleeding risk. OBJECTIVE: To review the risk of VTE and bleeding in pregnant and nulligravid women with KTS. METHODS: A retrospective medical record review was performed of women with KTS, aged ≥18 years, evaluated at Mayo Clinic Rochester, Minnesota, from August 1945 to April 2018. RESULTS: We identified 75 women with ≥1 pregnancy and 64 nulligravid women. VTE prevalence was 14 of 70 (20%) for women with a history of pregnancy and 16 of 64 (25%) for nulligravid women (P = .93). Among the 70 women with a history of pregnancy, 7 of 18 VTE events (39%) occurred in association with pregnancy, with VTE affecting 7 of 151 pregnancies (4.6%). Significant bleeding prevalence was 6 of 70 (8.6%) for women with a history of pregnancy and 6 of 64 (9.4%) for nulligravid women (P = .54). LIMITATIONS: This was a retrospective review. CONCLUSION: The prevalence of VTE and bleeding was similar in patients with KTS, irrespective of pregnancy status.


Asunto(s)
Hemorragia/etiología , Síndrome de Klippel-Trenaunay-Weber/diagnóstico , Resultado del Embarazo , Embarazo de Alto Riesgo , Tromboembolia Venosa/etiología , Centros Médicos Académicos , Adulto , Estudios de Cohortes , Bases de Datos Factuales , Femenino , Hemorragia/diagnóstico , Hemorragia/epidemiología , Humanos , Síndrome de Klippel-Trenaunay-Weber/complicaciones , Embarazo , Complicaciones del Embarazo/diagnóstico , Complicaciones del Embarazo/mortalidad , Embolia Pulmonar/epidemiología , Embolia Pulmonar/etiología , Embolia Pulmonar/fisiopatología , Estudios Retrospectivos , Medición de Riesgo , Tasa de Supervivencia , Malformaciones Vasculares/complicaciones , Malformaciones Vasculares/diagnóstico , Tromboembolia Venosa/diagnóstico , Tromboembolia Venosa/terapia , Adulto Joven
20.
Pediatr Dermatol ; 36(5): 741-742, 2019 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-31282007

RESUMEN

We investigated the impact of a personalized telephone call reminder for patients that had not confirmed their clinic appointment, in addition to automated reminders, on monthly no-show rates. Our data revealed a reduction in the monthly no-show rate from 16.0% (SD = 3.91%) before the intervention to 13.1% (SD = 0.27%, P = 0.0997) after the intervention, which was not statistically significant. The standard deviation of the no-show rate with the intervention was reduced, leading to a predictable monthly no-show rate (range 12.93%-13.51%). Thus, the number of patients attending clinic was more predictable. This study highlights the need for additional investigation of factors associated with appointment nonadherence in pediatric dermatology.


Asunto(s)
Instituciones de Atención Ambulatoria , Citas y Horarios , Dermatología , Pacientes no Presentados , Pediatría , Sistemas Recordatorios , Humanos , Proyectos Piloto , Teléfono
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA