Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Related Concept Videos

Prosopagnosia

Prosopagnosia

Prosopagnosia, also known as face blindness, is the inability to recognize faces. In severe cases, individuals with prosopagnosia may not recognize close family members, including parents and spouses, by their faces. For instance, someone with prosopagnosia might walk past their child in a crowd, only realizing their mistake upon noticing their child's distinctive backpack or favorite jacket. Prosopagnosia specifically impairs facial recognition, while the recognition of other objects or...

Neurulation

Neurulation

Neurulation is the embryological process which forms the precursors of the central nervous system and occurs after gastrulation has established the three primary cell layers of the embryo: ectoderm, mesoderm, and endoderm. In humans, the majority of this system is formed via primary neurulation, in which the central portion of the ectoderm—originally appearing as a flat sheet of cells—folds upwards and inwards, sealing off to form a hollow neural tube. As development proceeds, the anterior...

You might also read

Related Articles

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

Sort by

Same author

Sigmoid Lithobezoar associated with iron deficiency anaemia: a rare case report.

Oxford medical case reports·2025

Same author

Identification of molecular heterogeneity in telomere maintenance pathway of aplastic anemia.

Molecular biology reports·2025

Same author

A next-generation sequencing-based universal target panel and algorithm for one-stop detection of copy number alterations and single-nucleotide variations in the HBB gene cluster for rapid diagnosis of β-thalassemia.

Molecular biology reports·2025

Same author

Identification of a Novel Homozygous Missense Mutation in the CLDN16 Gene to Decipher the Ambiguous Clinical Presentation Associated with Autosomal Dominant Hypocalcaemia and Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis in an Indian Family.

Calcified tissue international·2023

Same author

Ten- vs. 14-day antibiotic therapy for culture-positive neonatal sepsis.

Journal of tropical pediatrics·2023

Same author

Role of cooked green banana in home management of acute diarrhea in under-5 children.

Journal of tropical pediatrics·2023

Search research articles

Related Experiment Video

Updated: Jul 8, 2026

Full-Endoscopic Surgery for Hypothalamic Hamartoma Resection

Full-Endoscopic Surgery for Hypothalamic Hamartoma Resection

Published on: April 12, 2024

Holoprosencephaly--a case report.

Hosenera Begum¹, Kaustav Nayek

¹Department of Paediatrics, Calcutta Medical College, Kolkata.

Journal of the Indian Medical Association

|January 9, 2008

Summary

A newborn presented with delayed breathing and a large monoventricle, indicating alobar holoprosencephaly with hydrocephalus. This rare congenital brain malformation requires prompt diagnosis and management.

Area of Science:

Neonatal neurology
Developmental neuroscience
Pediatric radiology

Background:

Delayed respiration in newborns can signify critical underlying conditions.
Holoprosencephaly is a spectrum of brain malformations resulting from incomplete forebrain division.

Observation:

A term newborn exhibited delayed respiration and an unusually large head circumference (40.5 cm).
Radiological imaging revealed significant sutural separation on skull X-ray.
Cranial CT scan demonstrated a large monoventricle occupying most of the brain cavity.

Findings:

The observed features are characteristic of alobar holoprosencephaly.
Concurrent hydrocephalus was identified as a significant complication.
The infant was managed for birth asphyxia.

More Related Videos

Frontal Disconnection for Treating Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Epilepsy (MOGHE) in the Frontal Lobe

Frontal Disconnection for Treating Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Epilepsy (MOGHE) in the Frontal Lobe

Published on: August 16, 2024

Related Experiment Videos

Last Updated: Jul 8, 2026

Full-Endoscopic Surgery for Hypothalamic Hamartoma Resection

Full-Endoscopic Surgery for Hypothalamic Hamartoma Resection

Published on: April 12, 2024

Frontal Disconnection for Treating Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Epilepsy (MOGHE) in the Frontal Lobe

Frontal Disconnection for Treating Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Epilepsy (MOGHE) in the Frontal Lobe

Published on: August 16, 2024

Implications:

Early identification of alobar holoprosencephaly with hydrocephalus is crucial for appropriate neonatal care.
This case highlights the importance of advanced neuroimaging in diagnosing complex congenital brain anomalies.
Understanding such malformations aids in counseling families and planning potential interventions.