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Related Concept Videos

Amyloid Fibrils03:03

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Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining,...
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Cortisol production is normally governed by the hypothalamic–pituitary–adrenal (HPA) axis, which maintains hormonal balance through tightly regulated feedback mechanisms. Disruption of this regulatory system is central to the development of Cushing syndrome, whether the excess cortisol originates from external medications or internal pathology. Persistent cortisol elevation alters metabolism, immune function, and endocrine signaling, producing the characteristic clinical features...
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Related Experiment Video

Updated: Apr 18, 2026

A Non-invasive Way to Isolate and Phenotype Cells from the Conjunctiva
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Conjunctival amyloidosis -- clinical and histopathologic features.

D Suesskind1, F Ziemssen, J M Rohrbach

  • 1Department of Ophthalmology, Eberhard Karls University Tuebingen, Schleichstr. 12-16, 72076, Tuebingen, Germany, daniela.suesskind@med.uni-tuebingen.de.

Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie
|January 27, 2015
PubMed
Summary

Conjunctival amyloidosis is a rare condition often misdiagnosed. Histopathology confirmed amyloidosis in six patients with unclear conjunctival lesions, highlighting the need for biopsy in suspicious cases.

Area of Science:

  • Ophthalmology
  • Pathology
  • Immunohistochemistry

Background:

  • Conjunctival amyloidosis is a rare disorder.
  • Often clinically unsuspected or misdiagnosed.
  • Requires thorough histopathological evaluation.

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