Combined alkaptonuria and osteoporosis contributing to chronic back pain
Alkaptonuria is a rare autosomal recessive metabolic disorder caused by a deficiency in homogentisate 1,2-dioxygenase (HGD), leading to the accumulation of homogentisic acid (HGA) in connective tissues, cartilage, and bones. This accumulation results in multisystem involvement, including early-onset...
Na minha lista:
| Principais autores: | , |
|---|---|
| 格式: | Artigo |
| 语言: | Inglês |
| 出版: |
Bioscientifica
2025-09-01
|
| 丛编: | Endocrinology, Diabetes & Metabolism Case Reports |
| 主题: | |
| 在线阅读: | https://edm.bioscientifica.com/view/journals/edm/2025/3/EDM-25-0071.xml |
| 标签: |
没有标签, 成为第一个标记此记录!
|