Abstract
A pair of male monozygotic twins, both affected by progeria is described. The concordance in this manifestation suggests a genetic aetiology and other evidence indicates the implication of autosomal recessive factors; the chromosomes of these patients show no detectable abnormalities.
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Selected References
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- Danes B. S. Progeria: a cell culture study on aging. J Clin Invest. 1971 Sep;50(9):2000–2003. doi: 10.1172/JCI106692. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Macnamara B. G., Farn K. T., Mitra A. K., Lloyd J. K., Fosbrooke A. S. Progeria. Case report with long-term studies of serum lipids. Arch Dis Child. 1970 Aug;45(242):553–560. doi: 10.1136/adc.45.242.553. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marcondes E., Campos J. V., Barbieri D., Quarentei G., Cavallo A. Progéria: relato de um caso com manifestaçes de esclerose sistêmica progressiva (esclerodermia) desde o nascimento. Rev Hosp Clin Fac Med Sao Paulo. 1969 Mar-Apr;24(2):147–154. [PubMed] [Google Scholar]

