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- W2018924277 abstract "Seckel syndrome is a rare, recessively inherited disorder of severe growth retardation and distinct craniofacial, orodental, and skeletal anomalies. Even though there are well-established minimum diagnostic criteria for this syndrome, controversy exists about its boundaries and criteria for exclusion. We studied 2 remarkably similar, unrelated children with most of the clinical and radiographic manifestations of Seckel's original patient. Although their craniofacial and orodental anomalies are typical of Seckel syndrome, 1 child has unusual appearance of the hands and feet that have not been previously associated with it. This patient appears to define a new Seckel-like syndrome and suggests heterogeneity in this type of primordial dwarfism." @default.
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- W2018924277 date "1996-08-23" @default.
- W2018924277 modified "2023-09-27" @default.
- W2018924277 title "A new Seckel-like syndrome of primordial dwarfism" @default.
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- W2018924277 doi "https://doi.org/10.1002/(sici)1096-8628(19960823)64:3<447::aid-ajmg1>3.0.co;2-m" @default.
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