Literature DB >> 1583660

Oculoauriculovertebral spectrum and cerebral anomalies.

C T Schrander-Stumpel1, C E de Die-Smulders, R C Hennekam, J P Fryns, P X Bouckaert, O F Brouwer, J J da Costa, E J Lommen, P D Maaswinkel-Mooy.   

Abstract

We report on three Dutch children with a clinical diagnosis of oculoauriculovertebral spectrum (OAVS) and hydrocephalus. The clinical features are compared to 15 published cases of OAVS and hydrocephalus. Several other cerebral abnormalities were present in the whole group. About half of the cases had cleft lip/palate, anophthalmia/microphthalmia, or a cardiac defect. Mental retardation was found in five of the surviving 11 patients and early death occurred in one-third. We compared the cases with OAVS and hydrocephalus with published reports of OAVS and other cerebral anomalies and found no significant clinical differences. However, the clinical characteristics were clearly more severely expressed than generally found in patients with OAVS. Children with OAVS and more severe clinical features, especially anophthalmia/microphthalmia and cleft lip/palate, seem to be at an increased risk for cerebral malformations and for mental retardation.

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Year:  1992        PMID: 1583660      PMCID: PMC1015953          DOI: 10.1136/jmg.29.5.326

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  23 in total

1.  Paroxysmal intracranial hypertension and oculoauriculovertebral dysplasia.

Authors:  R C Hennekam; O Van Nieuwenhuizen; R H Gooskens
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Journal:  Pediatrics       Date:  1990-08       Impact factor: 7.124

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Authors:  R Mettey; G Masson; M P Peyre; A Hoppeler
Journal:  J Genet Hum       Date:  1987-08

7.  Oculoauriculovertebral dysplasia and variants: phenotypic characteristics of 294 patients.

Authors:  B R Rollnick; C I Kaye; K Nagatoshi; W Hauck; A O Martin
Journal:  Am J Med Genet       Date:  1987-02

8.  Retinoic acid embryopathy.

Authors:  E J Lammer; D T Chen; R M Hoar; N D Agnish; P J Benke; J T Braun; C J Curry; P M Fernhoff; A W Grix; I T Lott
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Review 9.  Oculoauriculovertebral anomaly: variability and causal heterogeneity.

Authors:  B R Rollnick
Journal:  Am J Med Genet Suppl       Date:  1988

10.  Goldenhar syndrome, anterior encephalocele, and aqueductal stenosis following fetal primidone exposure.

Authors:  E E Gustavson; H Chen
Journal:  Teratology       Date:  1985-08
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  2 in total

1.  Oculocerebrocutaneous syndrome: the brain malformation defines a core phenotype.

Authors:  U Moog; M C Jones; L M Bird; W B Dobyns
Journal:  J Med Genet       Date:  2005-05-06       Impact factor: 6.318

2.  [Diffuse brain atrophy in a Goldenhar syndrome: report of a case].

Authors:  Yogolelo Asani; Cilundika Mulenga; Léon Kabamba Ngombe; Kalenga Muenze; Chenge Borasisi
Journal:  Pan Afr Med J       Date:  2014-10-13
  2 in total

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