Literature DB >> 2098044

Cerebral midline developmental anomalies: spectrum and associated features.

A L Delezoide1, F Narcy, J C Larroche.   

Abstract

Cerebral midline anomalies are defects of anatomical relationships between the two hemispheres. They include holoprosencephalies, septal and commissural agenesis. Agenesis of the olfactory tract (arhinencephalies) are often included in the spectrum of holoprosencephalies and the facial phenotype is thought to be affected and characteristic in the midline development abnormalities. This work concerns a review of the literature and personal experience in two units of Fetopathology in Paris. This study confirms the relationships between various cerebral malformations and their frequent association. However, arhinencephaly and moreover agenesis of corpus callosum should be considered as heterogeneous entities, often totally distinct and independent from the malformative process of the holoprosencephaly. In addition, if major facial anomalies such as cyclopia are almost pathognomonic for holoprosencephaly, minor malformations such as lateral facial clefts of cleft palates result from a great variety of malformative processes.

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Mesh:

Year:  1990        PMID: 2098044

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  5 in total

1.  Agnathia Holoprosencephaly and Situs Inversus in A Neonate Born to an Alcoholic Mother.

Authors:  Dibyajyoti Goswami; Giriraj Kusre
Journal:  J Clin Diagn Res       Date:  2015-05-01

2.  Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions.

Authors:  Luis Teixeira; Fabien Guimiot; Catherine Dodé; Catherine Fallet-Bianco; Robert P Millar; Anne-Lise Delezoide; Jean-Pierre Hardelin
Journal:  J Clin Invest       Date:  2010-10       Impact factor: 14.808

3.  Sek4 and Nuk receptors cooperate in guidance of commissural axons and in palate formation.

Authors:  D Orioli; M Henkemeyer; G Lemke; R Klein; T Pawson
Journal:  EMBO J       Date:  1996-11-15       Impact factor: 11.598

4.  Prenatal MRI findings of polycystic kidney disease associated with holoprosencephaly.

Authors:  Mustafa Koplay; Omer Onbas; Fatih Alper; Bunyamin Borekci
Journal:  Korean J Radiol       Date:  2009-04-22       Impact factor: 3.500

Review 5.  Holoprosencephaly.

Authors:  Christèle Dubourg; Claude Bendavid; Laurent Pasquier; Catherine Henry; Sylvie Odent; Véronique David
Journal:  Orphanet J Rare Dis       Date:  2007-02-02       Impact factor: 4.123

  5 in total

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