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Sanjad-Sakati Syndrome in Omani children
Sanjad Sakati Syndrome is an Autosomal Recessive disorder found exclusively in people of Arabian origin. It was first reported from the Kingdom of Saudi Arabia in 1988. This is a report of a family with this rare disease in Oman. The syndrome comprises of congenital hypoparathyroidism, severe growth...
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
OMJ
2010
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3191633/ https://ncbi.nlm.nih.gov/pubmed/22043344 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5001/omj.2010.63 |
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