These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Multiple synostosis syndrome: study of a large Brazilian kindred.
    Author: da-Silva EO, Filho SM, de Albuquerque SC.
    Journal: Am J Med Genet; 1984 Jun; 18(2):237-47. PubMed ID: 6465200.
    Abstract:
    We report a large Brazilian kindred with 28 cases of the autosomal dominant multiple synostosis syndrome. The main anomalies were symphalangism and carpal and tarsal synostoses. Other common findings included synostosis involving other bones, absence of phalanges and nails, short metacarpals, pes planovalgus with prominent lateral border, hypoplastic alae of nose, short upper lip, and dermatoglyphic abnormalities. This may be a variant of the WL syndrome.
    [Abstract] [Full Text] [Related] [New Search]