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- W2891901946 abstract "Seckel syndrome is a rare genetic disorder characterized by marked intra-uterine growth retardation (primordial dwarfism) and post natal dwarfism, microcephaly, mental retardation and typical facial features with a 'bird-headed' appearance. The syndrome has autosomal recessive inheritance with equal male and female sex occurrence. Here is an interesting case of a nineteen years old male patient, presented with various clinical manifestations, typical radiographic features and characteristic dental manifestations correlated with the literature. A thorough knowledge aids in better diagnosis, proper management and prevention of disastrous complications arising from this extremely rare inherited disorder, the Seckel syndrome." @default.
- W2891901946 created "2018-09-27" @default.
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- W2891901946 date "2018-01-01" @default.
- W2891901946 modified "2023-09-23" @default.
- W2891901946 title "Seckel syndrome: A case report of the rare syndrome" @default.
- W2891901946 doi "https://doi.org/10.4103/jdrntruhs.jdrntruhs_100_14" @default.
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