A5059105716- Systemic Sclerosis and Related Diseases
- Skin Diseases and Diabetes
- Skin and Cellular Biology Research
- Autoimmune Bullous Skin Diseases
- Dermatological and Skeletal Disorders
- Systemic Lupus Erythematosus Research
- Cutaneous Melanoma Detection and Management
- Contact Dermatitis and Allergies
- Neonatal skin health care
- Genetic and rare skin diseases.
- Nail Diseases and Treatments
- Dermatology and Skin Diseases
- Vascular Malformations and Hemangiomas
- Cancer and Skin Lesions
- Allergic Rhinitis and Sensitization
- Immunodeficiency and Autoimmune Disorders
- Mast cells and histamine
- Streptococcal Infections and Treatments
- Urticaria and Related Conditions
- Genital Health and Disease
- Eosinophilic Disorders and Syndromes
- Cutaneous lymphoproliferative disorders research
- Parvovirus B19 Infection Studies
- Dermatological and COVID-19 studies
- T-cell and B-cell Immunology
Texas Children's Hospital
2016-2025
Baylor College of Medicine
2016-2025
Baylor School
2019
Baylor University
2018
Children's Cancer Center
2017
Johns Hopkins Hospital
2016
Boston Children's Hospital
2015
New York University
2010-2013
Johns Hopkins University
2010
Sydney Children's Hospital
2000
Chronic skin disorders in children frequently are visible and can cause stigmatization. However, the extent of stigmatization from chronic disease association with mental health needs further study.
Erythema ab igne is a reticulated, erythematous or hyperpigmented dermatosis that results from chronic and repeated exposure to low levels of infrared radiation. Multiple heat sources have been reported cause this condition, which include heated reclining chairs, heating pads, hot water bottles, car heaters, electric space and, more recently, laptop computers. Treatment consists withdrawing the inciting source. Although erythema carries good prognosis, it not necessarily self-limited...
<h3>Importance</h3> Ulceration is a common complication of infantile hemangioma (IH), which leads to substantial morbidity. in IH has not been systematically studied since the advent β-blocker therapy for IH. <h3>Objectives</h3> To examine treatment interventions used ulceration and identify clinical prognostic indicators healing time. <h3>Design, Setting, Participants</h3> A retrospective, multicenter cohort study was conducted on 436 consecutive patients with diagnosis ulcerated available...
ABSTRACT An association between confluent and reticulated papillomatosis (CARP) obesity has been reported; however, the relationship CARP treatment response remains unknown. A retrospective chart review was performed of 92 pediatric patients diagnosed treated for during a 7‐year period at single institution. Twenty‐three non‐obese responded to therapy higher rate compared 69 obese (100% vs. 77.5%; p = 0.009) regardless duration, type, age, or sex, based on multivariable analysis. Our results...
Abstract Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome is a rare autoinflammatory disorder. Cutaneous manifestations of CANDLE include characteristic recurring violaceous annular plaques comprised an immature dermal mononuclear cell infiltrate. In syndrome, deleterious genetic mutations inhibit proteasome‐immunoproteasome function, resulting in cellular accumulation ubiquitinated waste proteins that activate type I interferon signaling...
To assess the management and outcomes of afebrile infants who received a pediatric dermatology consultation for pustules and/or vesicles.
Abstract Background Epidemiological knowledge and predictors of melanoma among children adolescents in multiethnic populations are limited. Procedure Using data from the Texas Cancer Registry (TCR) Surveillance, Epidemiology, End Results (SEER) 13 database, we identified incident cases diagnosed at 0–20 years old during 1995–2013 United States, respectively. negative binomial regression, associations between demographic factors incidence rates (IR) were evaluated by calculating rate ratios...
Children with discoid lupus erythematosus (DLE) are at risk for disfigurement and progression to systemic (SLE). Consensus is lacking regarding optimal care children DLE. The aim of this study was compare practice patterns among paediatric dermatologists/rheumatologists treating An online survey sent 292 rheumatologists in the Childhood Arthritis Rheumatology Research Alliance 200 dermatologists Pediatric Dermatology Alliance. defined as ≥ 70% agreement. Survey response rates were 38% (76...
A 36-year-old African man from Guinea with a history of albinism presented many-year scaling and erythema the face, neck, arms. The patient had light eyes, hair, skin. Physical examination showed extensive photodamage. skin biopsy specimen posterior aspect lower leg squamous-cell carcinoma in situ. most common types oculocutaneous (OCA), OCA 1 2, are autosomal recessive disorders pigmentation that commonly affect skin, ears. Photodamage cancers plague patients albinism. In Africa, where is...
The Cutaneous Lupus Erythematosus Disease Area and Severity Index (CLASI) is a reliable outcome measure for cutaneous lupus erythematosus (CLE) in adults used clinical trials. However, it has not been validated children, limiting trials paediatric CLE. This study aimed to validate the CLASI paediatrics. Eleven patients with CLE, six dermatologists rheumatologists participated. physicians were trained use Physician's Global Assessment (PGA), individually rated all using both tools. Each...
Hereditary fibrosing poikiloderma with tendon contracture, myopathy, and pulmonary fibrosis (POIKTMP; Online Mendelian Inheritance in Man number, 615704) is a recently described autosomal dominant condition due to FAM111B mutation. Hallmark cutaneous findings begin childhood include poikiloderma, photosensitivity, bullae on the extremities. Thin hair, sparse eyebrows, eczematous skin changes are reported. Dermatologists play crucial role diagnosing this genetic disorder, which presents...
We present an atypical case of familial benign chronic pemphigus (Hailey-Hailey disease) that manifested with relapsing, flaccid vesicles and erosions, which were limited to the upper chest, anterior aspect neck, aspects arms without intertriginous involvement. Although individual eruptions in this patient demonstrated asymmetry, relapses did not obey a segmental distribution. To best our knowledge, no other has been described symmetric lesions localized solely body prior history at commonly...
Multiple endocrine neoplasia type 1 (MEN1) is a familial tumor syndrome with autosomal dominant inheritance. Cutaneous tumors in MEN1, which include multiple angiofibromas, collagenomas, and lipomas can easily be overlooked because of their subtle appearance. As markers this syndrome, recognition the mucocutaneous manifestations MEN1 important order to facilitate early interdisciplinary care diagnosis associated internal disease both patients family members.
Ulceration is a common complication of infantile hemangioma (IH). Severe, persistent ulceration occurs in minority patients. This study aims to characterize the clinical features IH with aggressive (AU).Multicenter retrospective AU.Thirty-five patients AU were identified and included study. The majority occurred segmental (23/35, 65%). Segmental large (≥10 cm2 ; 16/23, 69%, p < .001) thin (<3 mm) superficial component (16/23, .001). Localized had thick (>3 (11/12, 92%, All diaper area (9/35)...