Literature DB >> 7444800

Craniosynostosis with associated cranial base anomalies: a morphologic and histologic study of affected like-sexed twins.

K C Woon, V G Kokich, S K Clarren, M M Cohen.   

Abstract

A set of like-sexed male twins with the same malformation syndrome and exhibiting identical anomalous alterations of the craniofacial complex were studied in detail. The right and left coronal and left lamboidal sutures were prematurely synostosed in both specimens. The cranial base exhibited a mediolateral asymmetry, with the right half larger than the left. The occipital bone demonstrated the greatest abnormality, including bilateral clefting of the basioccipital component and alterations in the size and shape of the exoccipital bone. In lateral view, the cranial base was flattened and the ventral flexure occurred between the two components of the basioccipital. The odontoid process of the second cervical vertebra was rotated anteroinferiorly and formed part of the cranial floor. Histologically, the bilateral clefts of the basioccipital bone were united by fibrous connective tissue, and the central area of union contained chondroid-like bone. The cartilaginous spheno-occipital synchondrosis and the epiphyseal cartilage of the finger demonstrated similar dystrophic alterations. The brain was normal but exhibited external cerebral deformation secondary to aberrant skull shape.

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Mesh:

Year:  1980        PMID: 7444800     DOI: 10.1002/tera.1420220105

Source DB:  PubMed          Journal:  Teratology        ISSN: 0040-3709


  5 in total

1.  Normal growth and development in a child with Baller-Gerold syndrome (craniosynostosis and radial aplasia).

Authors:  P Galea; J L Tolmie
Journal:  J Med Genet       Date:  1990-12       Impact factor: 6.318

2.  A case of Baller-Gerold syndrome following in vitro fertilization-embryo transfer.

Authors:  M Mihai; L Eitan; P Gad; L Daniela
Journal:  J Assist Reprod Genet       Date:  1996-01       Impact factor: 3.412

3.  The Baller-Gerold syndrome.

Authors:  L Van Maldergem; A Verloes; L Lejeune; Y Gillerot
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

Review 4.  Baller-Gerold syndrome associated with congenital portal venous malformation.

Authors:  R Savarirayan; P Tomlinson; E Thompson
Journal:  J Med Genet       Date:  1998-09       Impact factor: 6.318

Review 5.  Phenotypic variability in the Baller-Gerold syndrome: report of a mildly affected patient and review of the literature.

Authors:  F J Ramos Fuentes; L Nicholson; C I Scott
Journal:  Eur J Pediatr       Date:  1994-07       Impact factor: 3.183

  5 in total

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