Achondroplasia with seronegative spondyloarthropathy resulting in recurrent spinal stenosis : A case report

BACKGROUND: Achondroplasia is an autosomal dominant condition caused by the G380 mutation of the gene encoding fibroblast growth factor receptor 3 on chromosome 4P. The classical findings include rhizomelic extremities, short stature, and spinal stenosis involving the upper cervical and distal lumba...

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Vydáno v:Surg Neurol Int
Hlavní autoři: Sakhrekar, Rajendra, Hadgaonkar, Shailesh, Hadgaonkar, Manisha, Sancheti, Parag, Shyam, Ashok
Médium: Artigo
Jazyk:Inglês
Vydáno: Scientific Scholar 2021
Témata:
Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8326084/
https://ncbi.nlm.nih.gov/pubmed/34345494
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.25259/SNI_409_2021
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