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Multiple Allele Traits01:49

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Increased intracranial pressure (ICP) refers to a potentially life-threatening rise in pressure inside the skull. This usually happens when there is a major change in the volume of brain tissue, blood, or cerebrospinal fluid (CSF) — the three components inside the skull. According to the Monro-Kellie doctrine, if the volume of one component increases, the volumes of the other components must decrease to maintain normal pressure. If this does not happen, ICP rises.The process often begins with...
Cranial and Spinal Meninges01:19

Cranial and Spinal Meninges

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Cranial Meninges
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Sutures of the Skull01:22

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Related Experiment Video

Updated: Jun 22, 2026

Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry
08:23

Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry

Published on: November 5, 2019

Cranial involvement in sickle cell disease.

Ozlem Alkan1, Ebru Kizilkilic, Osman Kizilkilic

  • 1Department of Radiology, Faculty of Medicine, Baskent University, Ankara, Turkey. yalinozlem@hotmail.com

European Journal of Radiology
|June 16, 2009
PubMed
Summary

Cranial abnormalities are common in patients with sickle cell disease (SCD) and neurological symptoms. Early diagnosis of these devastating SCD complications is crucial for effective management.

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Last Updated: Jun 22, 2026

Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry
08:23

Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry

Published on: November 5, 2019

Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
05:23

Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload

Published on: March 14, 2017

Area of Science:

  • Neurology
  • Radiology
  • Hematology

Background:

  • Sickle cell disease (SCD) is a genetic blood disorder.
  • Neurological complications significantly impact SCD patient outcomes.
  • Cranial involvement represents a severe manifestation of SCD.

Purpose of the Study:

  • To investigate and characterize cranial findings in patients experiencing neurological symptoms associated with SCD.
  • To assess the prevalence and types of brain abnormalities in this patient cohort.

Main Methods:

  • A cohort of 50 consecutive patients with SCD and neurological symptoms was studied.
  • Brain Magnetic Resonance (MR) examinations were performed, including classic MR imaging, diffusion-weighted MR imaging, MR angiography, and MR venography.
  • Digital subtraction angiography was utilized in a subset of patients.

Main Results:

  • Cranial abnormalities were detected in 62% of SCD patients.
  • Common findings included ischemic lesions (32%), low marrow signal intensity (24%), and cerebral atrophy (24%).
  • Other observed abnormalities included subarachnoid hemorrhage, moya-moya pattern, posterior reversible encephalopathy, dural venous sinus thrombosis, and osteomyelitis.

Conclusions:

  • Cranial involvement is a significant and severe complication of sickle cell disease.
  • Prompt and precise diagnosis of cranial complications in SCD is essential for patient management.