| Literature DB >> 4040172 |
Abstract
Five children in whom a diagnosis of Seckel syndrome had previously been made were re-examined in the genetic unit. One child had classical Seckel syndrome, a sib pair had the features of the syndrome with less severe short stature, and in two children the diagnosis was not confirmed. Seckel syndrome is only one of a group of low birth weight microcephalic dwarfism and careful attention should be paid to fulfillment of the major criteria defined by Seckel before the diagnosis is made. There remains a heterogeneous group of low birth weight microcephalic dwarfism yet to be defined.Entities:
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Year: 1985 PMID: 4040172 PMCID: PMC1049424 DOI: 10.1136/jmg.22.3.192
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318