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Related Experiment Video

Updated: Jan 10, 2026

Functional Characterization of Endogenously Expressed Human RYR1 Variants

Functional Characterization of Endogenously Expressed Human RYR1 Variants

Published on: June 9, 2021

Reed Syndrome.

Pradeep Balineni¹, Abhay K Kattepur¹, Deepak Hongaiah²

¹Department of Surgical Oncology, R. L Jalappa Institute of Oncology, Sri Devaraj Urs Academy of Higher Education and Research, Tamaka, Kolar, Karnataka India.

Indian Journal of Surgical Oncology

|November 24, 2025

Summary

This summary is machine-generated.

Reed syndrome links multiple skin tumors and uterine fibroids, increasing cancer risk. Individuals with Reed syndrome require vigilant monitoring for renal cell carcinoma development.

Keywords:

Leiomyomatosis Lesions Reed syndrome

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Area of Science:

Oncology
Dermatology
Genetics

Background:

Reed syndrome is a rare genetic disorder.
It is characterized by the syndromic association of multiple cutaneous leiomyomas and uterine fibroids.
This condition predisposes individuals to developing renal cell carcinomas.

Purpose of the Study:

To describe the key features of Reed syndrome.
To highlight the association between leiomyomas, fibroids, and renal cell carcinoma.
To emphasize the need for surveillance in affected individuals.

Main Methods:

Case illustration of a patient with Reed syndrome.
Review of existing literature on Reed syndrome.
Discussion of diagnostic criteria and management.

Main Results:

The image depicts the characteristic features of Reed syndrome.
Confirmed association between cutaneous leiomyomas, uterine fibroids, and increased risk of renal cell carcinoma.
Highlighted the importance of early diagnosis and monitoring.

Conclusions:

Reed syndrome necessitates close medical surveillance.
Early detection of renal cell carcinoma is crucial for improved outcomes.
Further research into the genetic basis and optimal management of Reed syndrome is warranted.