Literature DB >> 3298394

Holoprosencephaly and related midline cerebral anomalies: a review.

R W Leech, R M Shuman.   

Abstract

We propose a simple pathogenetic mechanism that reduces a bewildering variety of central nervous system malformations to a manageable group sharing defects of midline prosencephalic growth. It is neither new nor innovative, but attempts to summarize many pathologic entities within a concept that accounts for known embryologic events and the sequence and timing of those events. We propose midline prosencephalic dysgenesis as a category of malformations including aprosencephaly, holoprosencephaly, septo-optic dysplasia, and agenesis of the corpus callosum.

Entities:  

Mesh:

Year:  1986        PMID: 3298394     DOI: 10.1177/088307388600100102

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  10 in total

1.  Neurosonographic abnormalities in chromosomal disorders.

Authors:  T E Herman; M J Siegel
Journal:  Pediatr Radiol       Date:  1991

2.  Single forebrain ventricle without prosencephaly: agenesis of the corpus callosum with dehiscent fornices.

Authors:  G A de León; M A Radkowski; F A Gutierrez
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

3.  The arterial pattern at the base of arhinencephalic and holoprosencephalic brains.

Authors:  J J van Overbeeke; B Hillen; C Vermeij-Keers
Journal:  J Anat       Date:  1994-08       Impact factor: 2.610

4.  Histopathological study of alobar holoprosencephaly. 2. Marginal glioneural heterotopia and other gliomesenchymal abnormalities.

Authors:  M Mizuguchi; Y Morimatsu
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

5.  Aprosencephaly: review of the literature and report of a case with cerebellar hypoplasia, pigmented epithelial cyst and Rathke's cleft cyst.

Authors:  T S Kim; S Cho; D W Dickson
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

6.  The midline craniofacial skeleton in holoprosencephalic fetuses.

Authors:  I Kjaer; J W Keeling; N Graem
Journal:  J Med Genet       Date:  1991-12       Impact factor: 6.318

7.  Olfactory anomalies in CHARGE syndrome: imaging findings of a potential major diagnostic criterion.

Authors:  J Blustajn; C F E Kirsch; A Panigrahy; I Netchine
Journal:  AJNR Am J Neuroradiol       Date:  2008-04-16       Impact factor: 3.825

8.  Septo-optic-dysplasia-schizencephaly. Radiographic and clinical features.

Authors:  K C Kuban; R L Teele; J Wallman
Journal:  Pediatr Radiol       Date:  1989

9.  3-D reconstruction of a human fetus with combined holoprosencephaly and cyclopia.

Authors:  Wolfgang H Arnold; Veronika Meiselbach
Journal:  Head Face Med       Date:  2009-06-29       Impact factor: 2.151

10.  Characterization of an Inherited Neurologic Syndrome in Toyger Cats with Forebrain Commissural Malformations, Ventriculomegaly and Interhemispheric Cysts.

Authors:  M K Keating; B K Sturges; S Sisó; E R Wisner; E K Creighton; L A Lyons
Journal:  J Vet Intern Med       Date:  2016-02-04       Impact factor: 3.333

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.