Nonfamilial cherubism in a 6-month-old infant: a case report
Abstract Background Cherubism is known as a very rare autosomal dominant familial disorder of childhood caused by a mutation in the SH3BP2 gene on 4p16.3. It has not yet been observed at birth and is usually diagnosed in children aged 2-7. Here, we present a non-hereditary case of cherubism at a ver...
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Main Authors: | Seyedeh Sedigheh Hamzavi (Author), Alireza Askari (Author), Rosemina Bahrololoom (Author), Maral Mokhtari (Author), Anahita Sanaei Dashti (Author), Fatemeh Yarmahmoodi (Author), Somaye Rashidi (Author) |
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Format: | Book |
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BMC,
2024-06-01T00:00:00Z.
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