Jove
Visualize
Contact Us
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

Related Experiment Videos

Congenital Wells syndrome

B Z Garty1, M Feinmesser, M David

  • 1Department of Pediatrics, Schneider Children's Medical Center of Israel, Petah Tiqva, Israel.

Pediatric Dermatology
|July 1, 1997
PubMed
Summary

This case study presents a unique instance of congenital Wells syndrome (eosinophilic cellulitis) appearing at birth. Subcutaneous nodules may be an early indicator of this condition in infants.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Homozygous deletion of RAG1, RAG2 and 5' region TRAF6 causes severe immune suppression and atypical osteopetrosis.

Clinical genetics·2016
Same author

Functional hyposplenism is an important and underdiagnosed immunodeficiency condition in children.

Acta paediatrica (Oslo, Norway : 1992)·2014
Same author

Anaphylaxis in Israel: experience with 92 hospitalized children.

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology·2010
Same author

MHC class 2 deficiency and X-linked agammaglobulinaemia in a consanguineous extended family.

International journal of immunogenetics·2009
Same author

Extended family studies for the identification of allogeneic stem cell transplant donors in Jewish and Arabic patients in Israel.

Pediatric transplantation·2005
Same author

Ganciclovir treatment in Ménétrier's disease.

Acta paediatrica (Oslo, Norway : 1992)·2003

Area of Science:

  • Dermatology
  • Pediatrics
  • Immunology

Background:

  • Eosinophilic cellulitis, also known as Wells syndrome, is an inflammatory skin condition.
  • Typically, Wells syndrome presents in adults, with fewer documented cases in pediatric populations.
  • Congenital onset of dermatological conditions is rare and warrants further investigation.

Observation:

  • A female infant presented with subcutaneous nodules on the scalp and trunk immediately after birth.
  • At six months of age, the infant developed characteristic skin swelling and erythema.
  • Lesions resolved spontaneously but exhibited recurrent episodes.

Findings:

  • This case represents a potential instance of congenital Wells syndrome, uniquely presenting at birth.
  • The mother reported significant medication intake during pregnancy, including iron, vitamins, and natural remedies.
  • The precise relationship between maternal medication use and the infant's condition remains speculative.

Implications:

  • Subcutaneous nodules could be a primary presenting sign of Wells syndrome in neonates and infants.
  • This case highlights the possibility of congenital Wells syndrome and its potential triggers.
  • Further research is needed to explore the link between prenatal exposures and congenital dermatoses.

Related Experiment Videos