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

The acrocallosal syndrome.

N Philip1, N Apicella, I Lassman

  • 1INSERM U.242, Hôpital d-Enfants de la Timone, Marseille, France.

European Journal of Pediatrics
|February 1, 1988
PubMed
Summary
This summary is machine-generated.

Acrocallosal syndrome, a rare genetic disorder, presents with distinctive facial features, limb abnormalities, and corpus callosum agenesis. This study suggests it may be inherited recessively, with pre-axial foot polydactyly not being a constant feature.

Related Experiment Videos

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

Beyond sense-specific processing: decoding texture in the brain from touch and sonified movement.

iScience·2023
Same author

The impact of movement sonification on haptic perception changes with aging.

Scientific reports·2021
Same author

First Report of Fusarium Head Blight on Winter Wheat in the Grand Duchy of Luxembourg.

Plant disease·2019
Same author

First Report of Wheat Leaf Rust in the Grand Duchy of Luxembourg and the Progress of its Appearance over the 2003-2008 Period.

Plant disease·2019
Same author

First Report of the Nivalenol Chemotype of Fusarium graminearum Causing Head Blight of Wheat in the Grand Duchy of Luxembourg.

Plant disease·2019
Same author

[IHC, FISH, CISH, NGS in non-small cell lung cancer: What changes in the biomarker era?]

Revue de pneumologie clinique·2018
Same journal

Cost-benefit analysis of nirsevimab for respiratory syncytial virus prevention in infants: a population-based study.

European journal of pediatrics·2026
Same journal

Consensus statement on the use of standardized early mobilization in pediatric patients admitted to pediatric intensive care units in Italy.

European journal of pediatrics·2026
Same journal

Ultrasound-guided midline catheters in the neonatal intensive care unit: a single-center pilot study.

European journal of pediatrics·2026
Same journal

Gastrointestinal pathogens in paediatric patients with diarrhoea during the COVID-19 pandemic in Spain: a multicentre molecular-based prospective study.

European journal of pediatrics·2026
Same journal

Low serum immunoglobulin levels in pediatric atopic dermatitis: association with disease severity and exploratory scores.

European journal of pediatrics·2026
Same journal

Safely developing respiratory care during emergency neonatal transport through systematic collection and analysis of detailed ventilator data.

European journal of pediatrics·2026
See all related articles

Area of Science:

  • Medical Genetics
  • Developmental Biology
  • Clinical Dysmorphology

Background:

  • Acrocallosal syndrome is a rare genetic disorder characterized by specific facial features, polydactyly, and agenesis of the corpus callosum.
  • Previous descriptions suggest pre-axial polydactyly of the feet as a consistent feature.