| Literature DB >> 3115102 |
M G Butler, B D Hall, R N Maclean, C B Lozzio.
Abstract
We report on a 12-yr-old female and a 14-yr-old male with Seckel syndrome. The 12-yr-old female had pancytopenia, which is seen occasionally in patients with Seckel syndrome and is also a feature of Fanconi anemia, a well-recognized autosomal recessive dwarfism syndrome with chromosome instability. Chromosome breakage analysis of both of our patients also indicated chromosome instability. We suggest that there may be a subgroup of Seckel syndrome patients with chromosome instability and/or hematological problems.Entities:
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Year: 1987 PMID: 3115102 PMCID: PMC5494982 DOI: 10.1002/ajmg.1320270318
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299