Benign neonatal hemangiomatosis

Related Experiment Video

Updated: Sep 21, 2026

A Comprehensive Procedure to Evaluate the In Vitro Performance of the Putative Hemangioblastoma Neovascularization Using the Spheroid Sprouting Assay
08:26

A Comprehensive Procedure to Evaluate the In Vitro Performance of the Putative Hemangioblastoma Neovascularization Using the Spheroid Sprouting Assay

Published on: April 12, 2018

Alexander K C Leung1, Massoud Rafaat

  • 1Department of Pediatrics, University of Calgary, Alberta, Canada. aleung@ucalgary.ca

Pediatric Dermatology
|March 27, 2003
PubMed

Abstract:

An infant with benign neonatal hemangiomatosis is described. Examination for internal hemangiomas was negative. The patient had complete resolution of the lesions by 2 years of age.

More Related Videos

Full-Endoscopic Surgery for Hypothalamic Hamartoma Resection
02:22

Full-Endoscopic Surgery for Hypothalamic Hamartoma Resection

Published on: April 12, 2024

Laparoscopic Anatomical Right Hemihepatectomy via the In Situ Anterior Approach
05:30

Laparoscopic Anatomical Right Hemihepatectomy via the In Situ Anterior Approach

Published on: August 8, 2025

Related Experiment Videos

Last Updated: Sep 21, 2026

A Comprehensive Procedure to Evaluate the In Vitro Performance of the Putative Hemangioblastoma Neovascularization Using the Spheroid Sprouting Assay
08:26

A Comprehensive Procedure to Evaluate the In Vitro Performance of the Putative Hemangioblastoma Neovascularization Using the Spheroid Sprouting Assay

Published on: April 12, 2018

Full-Endoscopic Surgery for Hypothalamic Hamartoma Resection
02:22

Full-Endoscopic Surgery for Hypothalamic Hamartoma Resection

Published on: April 12, 2024

Laparoscopic Anatomical Right Hemihepatectomy via the In Situ Anterior Approach
05:30

Laparoscopic Anatomical Right Hemihepatectomy via the In Situ Anterior Approach

Published on: August 8, 2025

Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...

Articles linked to this work by shared authors, journal, and citation graph.

Invasive Meningococcal Disease: A Hong Kong Perspective as a Low-incidence Asian City.

Current pediatric reviews·2026

Overview of Selective National Guidelines and Clinical Recommendations for Childhood Respiratory Syncytial Virus (RSV) Prophylaxis: A Hong Kong Perspective for Asia.

Current pediatric reviews·2026

Dual Viral Threats of Influenza and Emerging Chikungunya Fever in a Temperate City: Paediatric Perspectives.

Current pediatric reviews·2026

Expression and Correlation Analysis of Neuropeptide Family Members in the Peripheral Blood of Patients with COVID-19.

Current pediatric reviews·2026

A Narrative Review of Dietary Interventions and Supplementation for the Prevention and Treatment of Atopic Dermatitis.

Current pediatric reviews·2026

Infectious associations in childhood Kawasaki Disease.

Current pediatric reviews·2026

Fortuitous Discovery of Asymptomatic Homozygous Antithrombin Deficiency: A Rare p.Leu131Phe Heparin-Binding Site Mutation: A Case Report.

EJHaem·2026

Creatine metabolism is dysregulated in necrotizing enterocolitis.

Pediatric research·2026

Laparoscopic intravesical ureteroneocystostomy for pediatric vesicoureteral reflux: A comparison of Cohen and Politano-Leadbetter techniques.

Journal of pediatric urology·2026

Characterization of N-glycosylation remodeling in cerebrospinal fluid extracellular vesicles in children with purulent meningitis and viral meningitis: an exploratory glycomics study based on MALDI-TOF/TOF-MS.

Glycoconjugate journal·2026
See all related articles
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies
Jove
Visualize
Contact Us