Progeria in twins

Author:

Viegas J.,Souza P. L. R.,Salzano F. M.

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference5 articles.

1. Progeria: a cell culture study on aging;Danes, B.S.;Journal of Clinical Investigation,1971

2. The Hutchinson-Gilford progeria syndrome;De Busk, F.L.;J7ournal,1972

3. Progeria. Case report with long-term studies of serum lipids;Macnamara, G.P.; Farn, K.T.; Mitra, A.K.; Lloyd, J.K.; Fosbrooke, A.S.;Archives of Disease in Childhood,1970

4. Prog6ria. Revista do Hospital das Clinicas da Faculdade de Medicina de Sao;Marcondes, E.; Campos, J.V.M.; Barbieri, D.; Quarentei, G.; Cavallo, A.;Paulo,1969

5. The child was born at 38 weeks' gestation following a pregnancy complicated by emotional and social problems in an unwed mother for whom there was no prenatal care. Delivery was normal and the baby weighed 1900 g and had a length of 46 cm. She had several generalized seizures during the first few days of life which were interpreted as secondary to hypoglycaemia and responded to therapy with glucose. At 3 weeks of age, evaluation of failure to thrive revealed absence of a G-group chromosome. Subsequently the child continued to show re-

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