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Updated: Mar 7, 2026

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Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
Published on: June 8, 2022
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Lipoid Proteinosis (urbach-wiethe Disease)
Indian Journal of Dermatology, Venereology and Leprology
|February 15, 2017
Summary
This report details a rare case of lipoid proteinosis, a condition characterized by the buildup of hyaline material. The study highlights its infrequent occurrence in medical literature.
Area of Science:
- Dermatology
- Genetics
- Pathology
Background:
- Lipoid proteinosis, also known as hyalinosis cutis et mucosae or Urbach-Wiethe disease, is an extremely rare autosomal recessive disorder.
- It is characterized by the deposition of amorphous, hyaline-like material in the skin, mucous membranes, and internal organs.
Purpose of the Study:
- To report a rare case of lipoid proteinosis.
- To emphasize the infrequent occurrence of this condition.
Main Methods:
- Case report presentation.
- Review of existing medical literature on lipoid proteinosis.
Main Results:
- The case presented exhibits the typical clinical and pathological features of lipoid proteinosis.
- Literature review confirms the rarity of this disorder.
Conclusions:
- Lipoid proteinosis is a rare genetic disorder with significant clinical manifestations.
- Increased reporting of such rare cases aids in understanding its epidemiology and clinical spectrum.
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