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- W2005937634 abstract "Seckel syndrome, first defined by Seckel in 1960, is a rare (incidence 1:10,000), genetically heterogeneous autosomal recessive disorder presenting at birth. This syndrome is characterized by a proportionate dwarfism of prenatal onset, a severe microcephaly with a bird-headed like appearance (beaked nose, receding forehead, prominent eyes, and micrognathia), and mental retardation. The significance of dental alterations in this syndrome resides in the defect, hypoplastic enamel, being limited to the primary dentition; in most instances the second primary molar tooth is not affected. A case of the Seckel syndrome is presented." @default.
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- W2005937634 date "2012-01-01" @default.
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- W2005937634 title "Seckel syndrome: A report of a case" @default.
- W2005937634 doi "https://doi.org/10.4103/0970-4388.105021" @default.
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