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Kleeblattschädel syndrome: Difference between revisions

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Cloverleaf skull syndrome (''Kleeblattschädel'' syndrome) is a rare genetic disease, a deformity is etiologically and pathologically heterogeneous, so radical surgical reconstructive procedures should be planned and designed individually<ref>[https://www.jstage.jst.go.jp/article/nmc1959/31/2/31_2_87/_pdf Radical cranio-orbital reconstructive procedures for cloverleaf skull deformity in adult: operative technique for the longest survivor--case report]</ref>
Cloverleaf skull syndrome (''Kleeblattschädel'' syndrome) is a rare genetic disease, a deformity is etiologically and pathologically heterogeneous, so radical surgical reconstructive procedures should be planned and designed individually<ref>[https://www.jstage.jst.go.jp/article/nmc1959/31/2/31_2_87/_pdf Radical cranio-orbital reconstructive procedures for cloverleaf skull deformity in adult: operative technique for the longest survivor--case report]</ref>
'''Kleeblattschädel-Syndrom''' was first described by Holtermüller and Wiedermann in [[1960]]<ref>Oi et al. 1991</ref>
'''Kleeblattschädel-Syndrom''' was first described by [[K. Holtermüller|Holtermüller]] and [[H R. Widermann|Wiedermann]] in [[1960]]<ref>Oi et al. 1991 Neurol Med Chir (Tokyo):page 87</ref>


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Revision as of 15:29, 24 October 2015

Cloverleaf skull syndrome (Kleeblattschädel syndrome) is a rare genetic disease, a deformity is etiologically and pathologically heterogeneous, so radical surgical reconstructive procedures should be planned and designed individually[1] Kleeblattschädel-Syndrom was first described by Holtermüller and Wiedermann in 1960[2]