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

[Sarcoidosis].

J M van Proosdij1, J A Smeitink

  • 1Academisch Ziekenhuis Nijmegen.

Tijdschrift Voor Kindergeneeskunde
|April 1, 1989
PubMed
Summary
This summary is machine-generated.

Sarcoidosis is rare in children and presents with varied symptoms, often delaying diagnosis. This case study details a pediatric sarcoidosis patient

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

Corrigendum to "Mitochondrial and cytosolic thiol redox state are not detectably altered in isolated human NADH:ubiquinone oxidoreductase deficiency" [Biochim. Biophys. Acta. 2007;1772(9):1041-1051. PMID: 17600689].

Biochimica et biophysica acta. Molecular basis of disease·2021
Same author

Mining for mitochondrial mechanisms: Linking known syndromes to mitochondrial function.

Clinical genetics·2017
Same author

Recurrent acute liver failure and mitochondriopathy in a case of Wolcott-Rallison syndrome.

Journal of inherited metabolic disease·2008
Same author

A scale to monitor progression and treatment of mitochondrial disease in children.

Neuromuscular disorders : NMD·2006
Same author

Biochemical examination of fibroblasts in the diagnosis and research of oxidative phosphorylation (OXPHOS) defects.

Mitochondrion·2005
Same author

Prenatal diagnosis of NADH:ubiquinone oxidoreductase deficiency.

Prenatal diagnosis·2001
Same journal

Tijdschrift voor kindergeneeskunde·2020
Same journal

Tijdschrift voor kindergeneeskunde·2020
Same journal

Tijdschrift voor kindergeneeskunde·2020
Same journal

[The prematurely born child; should it be as early as possible?].

Tijdschrift voor kindergeneeskunde·1993
Same journal

[How do we continue?].

Tijdschrift voor kindergeneeskunde·1993
Same journal

[Child nutrition: what can still go wrong in the year 1992?].

Tijdschrift voor kindergeneeskunde·1993
See all related articles

Area of Science:

  • Pediatric Pulmonology
  • Immunology
  • Rare Diseases

Background:

  • Sarcoidosis is a multisystem inflammatory disease of unknown etiology.
  • Pediatric sarcoidosis is exceptionally rare, accounting for a small fraction of all sarcoidosis cases.
  • The diagnosis of sarcoidosis in children is challenging due to its infrequent occurrence and diverse clinical presentations.

Observation:

  • This report details a specific case of pediatric sarcoidosis.
  • The patient's clinical presentation was variable, complicating initial assessment.
  • Diagnostic challenges were encountered due to the atypical manifestation of the disease.

Findings:

  • The case illustrates the diagnostic difficulties associated with pediatric sarcoidosis.
  • A comprehensive diagnostic approach was necessary to confirm the sarcoidosis diagnosis.

Related Experiment Videos

  • The patient's therapeutic response and disease course are documented.

    • Implications:

    • Highlights the need for increased awareness of pediatric sarcoidosis among clinicians.
    • Emphasizes the importance of considering sarcoidosis in children with unexplained systemic symptoms.
    • Contributes to the understanding of sarcoidosis management in pediatric populations.