Familial hemifacial microsomia due to autosomal dominant inheritance. Case reports.

Hemifacial microsomia is a rare dentofacial anomaly which is regarded as a separate entity to Goldenhar syndrome and primarily affects the structures of the first branchial arch. It has a heterogeneous aetiology and tends to occur sporadically, though positive family histories have been reported. This paper reports on individuals in two generations of a family that has overlapping features of hemifacial microsomia and Goldenhar syndrome segregating as an autosomal dominant condition.

[1]  D. Wilson,et al.  Hemifacial microsomia: developmental consequence of perturbation of the auriculofacial cartilage model? , 1992, American journal of medical genetics.

[2]  J. Mulliken,et al.  A retrospective analysis of growth of the constructed condyle-ramus in children with hemifacial microsomia. , 1989, Cleft Palate Journal.

[3]  C. Kaye,et al.  Oculoauriculovertebral spectrum: an updated critique. , 1989, The Cleft palate journal.

[4]  R. Goldberg,et al.  The association of facial palsy and/or sensorineural hearing loss in patients with hemifacial microsomia. , 1989, The Cleft palate journal.

[5]  W. Hauck,et al.  Oculoauriculovertebral dysplasia and variants: phenotypic characteristics of 294 patients. , 1987, American journal of medical genetics.

[6]  K. Vargervik,et al.  Factors affecting long-term results in hemifacial microsomia. , 1986, The Cleft palate journal.

[7]  P. Fernhoff,et al.  Retinoic acid embryopathy. , 1985, The New England journal of medicine.

[8]  H. Chen,et al.  Goldenhar syndrome, anterior encephalocele, and aqueductal stenosis following fetal primidone exposure. , 1985, Teratology.

[9]  I. Ariel,et al.  Tracheo-oesophageal anomalies in the Goldenhar anomalad. , 1985, Journal of medical genetics.

[10]  J. Opitz,et al.  Hemifacial microsomia and variants: pedigree data. , 1983, American journal of medical genetics.

[11]  J. Marsh,et al.  Familial hemifacial microsomia. , 1983, The Cleft palate journal.

[12]  S. Clarren,et al.  Familial occurrence of hemifacial microsomia with radial limb defects. , 1982, American journal of medical genetics.

[13]  V. Godel,et al.  Further evidence for an autosomal dominant form of oculoauriculovertebral dysplasia , 1982, Clinical genetics.

[14]  D. Poswillo Otomandibular deformity: pathogenesis as a guide to reconstruction. , 1974, Journal of maxillofacial surgery.

[15]  P. J. Coccaro,et al.  THE CORRECTIVE TREATMENT OF THE SKELETAL ASYMMETRY IN HEMIFACIAL MICROSOMIA , 1973, Plastic and reconstructive surgery.

[16]  P. B. Wollschlaeger,et al.  Familial facial dysplasia. , 1970, Archives of ophthalmology.

[17]  S. Pruzansky,et al.  Not all dwarfed mandibles are alike , 1969 .

[18]  W. Grabb THE FIRST AND SECOND BRANCHIAL ARCH SYNDROME , 1965, Plastic and reconstructive surgery.

[19]  T. Rosendal Aplasia-Hypoplasia of the Otic Labyrinth after Thalidomide , 1965, Acta radiologica: diagnosis.