Literature DB >> 16879033

Meckel-Gruber syndrome: pathologic manifestations, minimal diagnostic criteria, and differential diagnosis.

Borislav A Alexiev1, Xiaoqing Lin, Chen-Chih Sun, David S Brenner.   

Abstract

This article provides an overview of the major pathologic manifestations of Meckel-Gruber syndrome, current knowledge about its pathogenesis, minimal diagnostic criteria, and differential diagnosis. Typical sonographic findings (occipital encephalocele, postaxial polydactyly, and cystic enlargement of the kidneys) allow for diagnosis of most cases before the 14th week of gestation, but the pathologist may encounter clinically unsuspected or atypical cases that require morphologic confirmation. In these cases, a meticulous autopsy is necessary to establish the diagnosis of Meckel-Gruber syndrome.

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Year:  2006        PMID: 16879033     DOI: 10.5858/2006-130-1236-MS

Source DB:  PubMed          Journal:  Arch Pathol Lab Med        ISSN: 0003-9985            Impact factor:   5.534


  25 in total

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Review 7.  Inherited cerebrorenal syndromes.

Authors:  Scott J Schurman; Steven J Scheinman
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Authors:  Zakia A Abdelhamed; Gabrielle Wheway; Katarzyna Szymanska; Subaashini Natarajan; Carmel Toomes; Chris Inglehearn; Colin A Johnson
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9.  Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis).

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10.  Functional redundancy of the B9 proteins and nephrocystins in Caenorhabditis elegans ciliogenesis.

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