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Kenny-Caffey syndrome type 1 in an Egyptian girl
Kenny-Caffey syndrome type 1 (KCS1) (OMIM 244460) is a rare syndrome characterized by growth retardation, uniformly small slender long bones with medullary stenosis, thickened cortex of the long bones, hypocalcemia possibly with tetany at an early age and normal intelligence. The primary outcome of...
Wedi'i Gadw mewn:
| Prif Awduron: | , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
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Medknow Publications & Media Pvt Ltd
2012
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3475915/ https://ncbi.nlm.nih.gov/pubmed/23087875 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2230-8210.100645 |
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