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Genes, crianças e pediatras: osteodistrofia hereditária de Albright
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Autores
Orientador(es)
Resumo(s)
A 11 month-old-year boy presented
with moon shaped face, limb shortening,
deformity of hands and feets, low stature
with weight on percentile 95, without macrocephaly.
Analytically he presented with
hypocalcaemia, hyperphosphatasemia and
high parathormone. The skeleton x-ray
did not show bone dysplasia. The typical
phenotype led to the diagnosis of Osteodistrophy of Albright.
Descrição
Palavras-chave
Osteodistrophy of Albright
Contexto Educativo
Citação
Nascer e Crescer 2010; 19(3): 180-181