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Ataxia telangiectasia: A report of two cousins and review of literature
Ataxia telangiectasia (AT) is a rare multisystem, neurodegenerative genetic disorder. Due to its wide clinical heterogeneity, it often leads physicians to an incorrect or missed diagnosis, and insight into this rare disease is important. Here is a case report of two cousins from the same family who...
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| Huvudupphovsmän: | , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Medknow Publications & Media Pvt Ltd
2011
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3343250/ https://ncbi.nlm.nih.gov/pubmed/22563157 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-5851.95145 |
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