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

Search research articles

Related Experiment Videos

[Hydranencephaly: report of a case].

M Badiane¹, M Ba, B Camara

¹Service de radiologie, CHU Fann.

Dakar Medical

|January 1, 1989

Summary

This report details the first documented case of hydranencephaly in Senegal, a rare brain deformity. Transfrontal echography proved effective for diagnosing this condition in a neonate.

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

Implementing a pragmatic randomised controlled trial in a humanitarian setting: lessons learned from the TISA trial.

Trials·2024

Same author

[Upperurinary Tract Diversion With JJ Stent By Endoscopy : Indications, Results And Morbidity].

Le Mali medical·2023

Same author

Temporal judgments of actions following unilateral brain damage.

Scientific reports·2022

Same author

Nebulised liposomal amphotericin-B as maintenance therapy in allergic bronchopulmonary aspergillosis: a randomised, multicentre trial.

The European respiratory journal·2021

Same author

Impact of seasonal malaria chemoprevention in children aged 3 to 59 months in the Kangaba and Kolokani health districts between 2013 and 2015.

Revue malienne d'infectiologie et de microbiologie·2021

Same author

Complete genome sequence of the marine Rhodococcus sp. H-CA8f isolated from Comau fjord in Northern Patagonia, Chile.

Marine genomics·2020

Area of Science:

Neurology
Pediatrics
Medical Imaging

Background:

Hydranencephaly is a rare congenital brain malformation characterized by the absence of cerebral hemispheres.
This condition presents significant diagnostic challenges, particularly in resource-limited settings.

Observation:

A three-week-old infant in Senegal presented with symptoms suggestive of a severe neurological abnormality.
Clinical examination revealed macroscopic signs consistent with a significant cranial and cerebral developmental anomaly.

Findings:

Transfrontal echography was utilized for diagnostic imaging, providing clear visualization of the cranial structures.
The diagnostic findings confirmed hydranencephaly, noting the near-complete absence of brain parenchyma and presence of cerebrospinal fluid within the cranial vault.

Implications:

This case highlights the importance of recognizing rare congenital anomalies in pediatric populations.
The successful use of transfrontal echography underscores its utility as a primary diagnostic tool for severe brain malformations, even in settings with limited advanced imaging resources.
Establishing the incidence of such rare conditions in specific geographic regions is crucial for public health planning and genetic counseling.

Related Experiment Videos