Smith–Fineman–Myers syndrome
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Smith–Fineman–Myers syndrome (SFMS1) is a congenital disorder that causes birth defects. This syndrome was named after Richard D. Smith, Robert M. Fineman and Gart G. Myers who discovered it around 1980.[3]
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Quick Facts Other names ...
Smith–Fineman–Myers syndrome | |
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Other names | X-linked mental retardation-hypotonic facies syndrome 1 (MRXHF1), Carpenter–Waziri syndrome, Chudley–Lowry syndrome, SFMS, Holmes–Gang syndrome and Juberg–Marsidi syndrome (JMS),[1][2] |
Smith–Fineman–Myers syndrome has an X-linked recessive pattern of inheritance. |
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