%0 Journal Article
%T Voc¨º conhece esta s¨ªndrome?
%A Lima
%A Livia Lima de
%A Ribas
%A Carla Barros da Rocha
%A Pereira
%A Priscilla Maria Rodrigues
%A Schettini
%A Renata Almeida
%A Eiras
%A Josie da Costa
%J Anais Brasileiros de Dermatologia
%D 2011
%I Sociedade Brasileira de Dermatologia
%R 10.1590/S0365-05962011000100031
%X huntchinson-gilford syndrome (progeria) is a rare autosomal dominant disease characterized by premature aging. it is reported the case of child whose alopecia started at the age of 6 months on the occipital region. the child also presented scleroderma plaques on the abdomen. this syndrome presents alterations in many organs and systems such as the skin and the skeletal and cardiovascular systems. the diagnosis is clinical and there is no treatment for it but recognition is necessary to minimize early atherosclerosis through the control of dyslipidemia.
%K aging
%K aging
%K premature
%K diagnosis
%K progeria.
%U http://www.scielo.br/scielo.php?script=sci_abstract&pid=S0365-05962011000100031&lng=en&nrm=iso&tlng=en