Exploring the genetic alterations of Gorham-Stout disease
The “vanishing bone disease” or Gorham-Stout disease (GSD) is a very rare disorder characterized by massive lymphatic and angiomatous proliferation accompanied by progressive osteolysis, without the deposition of new bone matrix. Because of its rare and complex clinical features, diagnosis is challe...
Saved in:
| Main Authors: | Olivia Pagliarosi, Jessica Pepe, Andrea Del Fattore, Michela Rossi |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2025-08-01
|
| Series: | Frontiers in Endocrinology |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fendo.2025.1654497/full |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
GORHAM-STOUT SYNDROME: DESCRIPTION OF A CASE
by: Elvira Nikolayevna Otteva, et al.
Published: (2010-08-01) -
Gorham Stout syndrome in a pediatric patient. A case report
by: Ariel Moya Machado, et al.
Published: (2023-03-01) -
Clinical features and current management experience in Gorham-Stout disease: a systematic review
by: Zilong Zhou, et al.
Published: (2025-03-01) -
Surgical treatment of Gorham-Stout disease combined with scoliosis: a case report and literature review
by: Yang Jiao, et al.
Published: (2024-12-01) -
Effective management of refractory chylothorax associated with elderly onset Gorham-Stout disease: A case report
by: Haruna Yamaki, et al.
Published: (2025-01-01)