Loading...
Leri-Weill Dyschondrosteosis Syndrome: Analysis via 3DCT Scan
Background: Leri-Weill dyschondrosteosis (LWD) is a pseudoautosomal form of skeletal dysplasia, characterized by abnormal craniofacial phenotype, short stature, and mesomelia of the upper and lower limbs. Methods: We describe two female patients with LWD. Their prime clinical complaints were severe...
Na minha lista:
| Udgivet i: | Medicines (Basel) |
|---|---|
| Main Authors: | , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
MDPI
2019
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6631815/ https://ncbi.nlm.nih.gov/pubmed/31146331 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/medicines6020060 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|