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Weill-Marchesani syndrome: report of an unusual case.
Giordano, N; Senesi, M; Battisti, E; Mattii, G; Gennari, C.
Afiliação
  • Giordano N; Institute of Internal Medicine and Medical Pathology University of Siena, viale Bracci 1, 53100 Siena, Italy.
Calcif Tissue Int ; 60(4): 358-60, 1997 Apr.
Article em En | MEDLINE | ID: mdl-9075633
We report a single case of Weill-Marchesani syndrome, typically characterized by progressive joint stiffness, brachiymorphy, brachydactyly, and ectopia lentis. The clinical case appears particularly interesting as the patient also had primary osteoporosis, which until now has not been considered as a possible manifestation of Weill-Marchesani syndrome.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoporose / Doenças do Tecido Conjuntivo / Nanismo Tipo de estudo: Diagnostic_studies Limite: Adult / Humans / Male Idioma: En Revista: Calcif Tissue Int Ano de publicação: 1997 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoporose / Doenças do Tecido Conjuntivo / Nanismo Tipo de estudo: Diagnostic_studies Limite: Adult / Humans / Male Idioma: En Revista: Calcif Tissue Int Ano de publicação: 1997 Tipo de documento: Article