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Encephalitis l: Introduction01:19

Encephalitis l: Introduction

Encephalitis is inflammation of the brain parenchyma, most often due to infections or autoimmune processes. It presents with neuropsychiatric features such as fever, altered mental status, behavioral changes, cognitive dysfunction, seizures, focal deficits, and sometimes autonomic instability. In some cases, the meninges are also involved, resulting in meningoencephalitis.Infectious CausesInfectious encephalitis is most commonly viral but can also result from bacterial, fungal, or parasitic...
Encephalitis ll: Pathophysiology01:26

Encephalitis ll: Pathophysiology

Encephalitis is inflammation of the brain parenchyma caused by direct viral invasion or immune-mediated mechanisms triggered by infections or tumors. Both processes lead to neuronal injury, disrupted neurotransmission, and diverse neurological symptoms, often with overlapping clinical and pathological features.Autoimmune EncephalitisIn autoimmune encephalitis, antibodies target neuronal antigens on cell surfaces, synapses, or within neurons. A key example is anti-NMDAR encephalitis, which can...
Hepatic Encephalopathy01:29

Hepatic Encephalopathy

DefinitionHepatic encephalopathy is a reversible neurologic syndrome that results from advanced liver dysfunction or portosystemic shunting. It leads to disturbances in cognition, behavior, and motor function due to the brain’s exposure to gut-derived toxins that the liver fails to detoxify.EtiologyThis condition develops either in the setting of acute fulminant hepatitis or progressively during chronic liver disease, such as cirrhosis and portal hypertension. Portosystemic shunting—including...
Cerebral Edema ll: Pathophysiology01:22

Cerebral Edema ll: Pathophysiology

Vasogenic edema is a major form of cerebral edema characterized by abnormal accumulation of fluid in the brain’s extracellular space due to disruption of the blood–brain barrier (BBB). The BBB is a specialized structure composed of endothelial cells connected by tight junctions, supported by astrocytic endfeet and a basement membrane. Under normal conditions, it tightly regulates the movement of ions, proteins, and solutes between the bloodstream and brain parenchyma. When this barrier loses...
Arboviral Encephalitis01:25

Arboviral Encephalitis

Arboviral encephalitis refers to brain inflammation caused by arthropod-borne viruses, particularly those transmitted through mosquito vectors. Among these, West Nile virus (WNV), a member of the Flaviviridae family, is a significant public health concern. WNV is an enveloped, positive-sense, single-stranded RNA virus. Human infection typically begins when an infected mosquito introduces the virus into the dermis during feeding. The primary transmission cycle involves birds as amplifying hosts...
Viral Meningitis01:18

Viral Meningitis

Viral meningitis is the most common form of meningitis and is often referred to as aseptic meningitis to indicate the absence of bacterial involvement. It is generally milder than bacterial meningitis, with symptoms including fever, headache, stiff neck, drowsiness, nausea, photophobia, and vomiting. Rarely, more severe manifestations or death may occur. Common causative agents include enteroviruses, particularly coxsackie A and B viruses and echoviruses, all members of the Enterovirus genus...

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Related Experiment Video

Updated: May 24, 2026

Mouse Models of Periventricular Leukomalacia
06:24

Mouse Models of Periventricular Leukomalacia

Published on: May 18, 2010

Leukoencephalopathies associated with macrocephaly.

Deborah L Renaud1

  • 1Division of Child and Adolescent Neurology, Department of Neurology, Mayo Clinic, Rochester, Minnesota 55901, USA. renaud.deborah@mayo.edu

Seminars in Neurology
|March 17, 2012
PubMed
Summary
This summary is machine-generated.

Macrocephaly, or enlarged head size, can indicate various conditions. When accompanied by white matter abnormalities, genetic leukoencephalopathies are suspected, requiring further investigation.

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Area of Science:

  • Neurology
  • Genetics
  • Pediatrics

Background:

  • Macrocephaly (enlarged head size) is a clinical sign observed in diverse conditions.
  • Benign familial macrocephaly is an inherited condition without neurological deficits.
  • Abnormal white matter on neuroimaging in macrocephalic individuals suggests underlying genetic disorders.

Purpose of the Study:

  • To outline key genetic leukoencephalopathies associated with macrocephaly and white matter abnormalities.
  • To differentiate benign familial macrocephaly from pathological causes.

Main Methods:

  • Review of clinical and neuroimaging findings in macrocephalic patients.
  • Genetic analysis and literature review for associated leukoencephalopathies.

Main Results:

  • Macrocephaly can be associated with hydrocephalus, genetic syndromes, or benign familial forms.
  • Specific genetic leukoencephalopathies to consider include Alexander's disease, Canavan's disease, CACH/VWMD, glutaric aciduria type I, L2-hydroxyglutaric aciduria, and MLC.

Conclusions:

  • Macrocephaly with abnormal white matter warrants consideration of specific genetic leukoencephalopathies.
  • Accurate diagnosis is crucial for appropriate management and genetic counseling.