A Case Report of Cardiac Ascites in Morquio Syndrome Complicated by Pulmonary Hypertension
Morquio syndrome, or mucopolysaccharidosis type IV (MPS IV), is a rare lysosomal storage disorder characterized by skeletal dysplasia and dysostosis multiplex. While primarily associated with skeletal manifestations, MPS IV can also affect systemic organs. Here, we present a case of a 64-year-old wo...
Saved in:
| Main Authors: | Gauri Patel, Olakanmi Joseph Deleawe |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
American College of Physicians
2025-03-01
|
| Series: | Annals of Internal Medicine: Clinical Cases |
| Online Access: | https://www.acpjournals.org/doi/10.7326/aimcc.2024.0579 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A Description of Skeletal Manifestation in Adult Case of Morquio Syndrome: Radiographic and MRI Appearance
by: Annalisa Di Cesare, et al.
Published: (2012-01-01) -
Clinical Characteristics of a Patient with Mucopolysaccharidosis Type IVA (Morquio Syndrome)
by: Nato D. Vashakmadze, et al.
Published: (2023-01-01) -
Rare Case of Morquio Syndrome (Mucopolysaccharidosis Type IVA): Difficulties of Diagnostic Search and Management
by: Yulia P. Semschikova, et al.
Published: (2022-03-01) -
Heliox in the management of respiratory failure in a Morquio A syndrome patient with trachea narrowing
by: Minghan Shi, et al.
Published: (2025-01-01) -
A case report of chylous ascites after cardiac surgery
by: Shuaishuai Yuan, et al.
Published: (2024-03-01)