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Camurati Engelmann Disease

Camurati-Engelmann DiseaseDiaphyseal dysplasia
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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Camurati Engelmann Disease" returned 1 free, full-text review articles. First 1 results:
Hypothalamic amenorrhea in a Camurati-Engelmann disease--a case report.
Last Updated: Nov 25, 2016

A case report of a patient diagnosed with Camurati-Engelmann Disease (CED) in association with the functional hypothalamic amenorrhea disturbances. CED is a very rare genetically determined disorder classified as a type of bone dysplasia.

Skull base manifestations of Camurati-Engelmann disease.
Last Updated: Nov 25, 2016

To describe presenting symptoms, evaluation findings, and surgical management of cranial base hyperostosis in patients with Camurati-Engelmann disease (CED).

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1 Free Review Articles 5 Review Articles

Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Camurati Engelmann Disease" returned 0 free, full-text editorial articles. First 0 results:
No publications were found for this category.
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Camurati Engelmann Disease" returned 24 free, full-text research articles. First few results:
Bone-targeted delivery of TGF-β type 1 receptor inhibitor rescues uncoupled bone remodeling in Camurati-Engelmann disease.
Last Updated: Aug 13, 2019

Camurati-Engelmann disease (CED) is a genetic bone-modeling disorder mainly caused by mutations in the gene that encodes transforming growth factor-β1 (TGF-β1). Symptoms of CED include bone pain, fractures, and dysplasia. Currently, effective therapies for bone fracture and dysplasia ...

Total Hip Arthroplasty in a Patient with Camurati-Engelmann Disease: A Case Report.
Last Updated: Nov 18, 2019

We review the case of a 44-year-old man with Camurati-Engelmann disease, who presented with chronic right hip pain that did not improve following intra-articular hip injections. He was functionally debilitated because of the worsening pain. Routine radiographs demonstrated severe ...

Clinical characteristics and treatment outcomes in Camurati-Engelmann disease: A case series.
Last Updated: Nov 14, 2018

Camurati-Engelmann disease is an extremely rare disease characterized by hyperostosis of multiple long bones. This condition is caused by heterozygous mutations in the TGFB1 gene.

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24 Free Research Articles 67 Research Articles