F.N. Nur Şeniz

487

the meckel syndrome: A case report and review of literature

the meckel syndrome: A case report and review of literature

The Meckel syndrome is a rare, autosomal recessive disease. Although the diagnostic criteria are still unclear, it has been suggested that at least 2 of the 3 abnormalities (i.e.central nervous system anomaly, polycystic kidneys and postaxial polydactyly) should be present to establish the diagnosis. This report presents the pathologic findings in a stillborn female with the Meckel syndrome from Diyarbakır.

Keywords:

Meckel syndrome, encepholocele, polycystic kidney congenital malformations,

Marmara Medical Journal-Cover

ISSN: 1019-1941
Yayın Aralığı: Yılda 3 Sayı
Başlangıç: 1988
Yayıncı: Marmara Üniversitesi

Arşiv

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