Literature DB >> 6161473

Severe fetal manifestation of hemifacial microsomia.

B Putz, H Rehder, R Grosspietzsch.   

Abstract

Hemifacial microsomia is a heterogenous complex lesion including predominantly unilateral face and head malformations mainly in the region of the first and second branchial arch, vertebral anomalies and varying accompanying malformations. A severe manifestation of this condition is demonstrated in a fetus by means of 5 mm thick sections of the whole head. Abortion had been induced because extreme microcephaly simulated fetal anencephaly in prenatal ultrasound examination. Alpha-Fetoprotein values were normal.

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Year:  1980        PMID: 6161473     DOI: 10.1007/BF00454836

Source DB:  PubMed          Journal:  Virchows Arch A Pathol Anat Histol        ISSN: 0340-1227


  7 in total

Review 1.  OCULOAURICULOVERTEBRAL DYSPLASIA.

Authors:  R J GORLIN; K L JUE; U JACOBSEN; E GOLDSCHMIDT
Journal:  J Pediatr       Date:  1963-11       Impact factor: 4.406

2.  Lateral facial dysplasia (first and second branchial arch syndrome, hemifacial microsomia).

Authors:  R B Ross
Journal:  Birth Defects Orig Artic Ser       Date:  1975

3.  The mandibulofacial dysostosis; a new hereditary syndrome.

Authors:  A FRANCESCHETTI; D KLEIN
Journal:  Acta Ophthalmol (Copenh)       Date:  1949

4.  Otomandibular deformity: pathogenesis as a guide to reconstruction.

Authors:  D Poswillo
Journal:  J Maxillofac Surg       Date:  1974-08

5.  The pathogenesis of the first and second branchial arch syndrome.

Authors:  D Poswillo
Journal:  Oral Surg Oral Med Oral Pathol       Date:  1973-03

6.  Ocular aspects of Goldenhar's syndrome.

Authors:  J L Baum; M Feingold
Journal:  Am J Ophthalmol       Date:  1973-02       Impact factor: 5.258

Review 7.  The first and second branchial arch syndrome.

Authors:  W C Grabb
Journal:  Plast Reconstr Surg       Date:  1965-11       Impact factor: 4.730

  7 in total

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