[Goldenhar syndrome: apropos of 2 cases]. 1990

A Medina Banegas, and M Gil Vélez, and J M Osete Albaladejo, and F Argudo Marco, and J Díaz-Yelo
Servicio de ORL, Hospital Virgen del Castillo, Yecla, Murcia.

The arc branch syndrome are a group of diseases whose classification and etiology are unknown yet. We has 2 patients with Goldenhar's syndrome and we have studied the etiopathogenicity and treatment in these diseases.

UI MeSH Term Description Entries
D008297 Male Males
D008342 Mandibulofacial Dysostosis A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized by a slant of the palpebral fissures, COLOBOMA of the lower lid, MICROGNATHIA and hypoplasia of the ZYGOMATIC ARCHES, and CONGENITAL MICROTIA. It is transmitted as an autosomal trait. The incomplete form (Treacher Collins syndrome) is characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (Dorland, 27th ed) MFD1 Mandibulofacial Dysostosis,Treacher Collins Syndrome,Franceschetti-Zwahlen-Klein Syndrome,Mandibulofacial Dysostosis (MFD1),Treacher Collins-Franceschetti Syndrome,Dysostoses, MFD1 Mandibulofacial,Dysostoses, Mandibulofacial,Dysostoses, Mandibulofacial (MFD1),Dysostosis, MFD1 Mandibulofacial,Dysostosis, Mandibulofacial,Dysostosis, Mandibulofacial (MFD1),Franceschetti Zwahlen Klein Syndrome,Franceschetti-Zwahlen-Klein Syndromes,MFD1 Mandibulofacial Dysostoses,Mandibulofacial Dysostoses,Mandibulofacial Dysostoses (MFD1),Mandibulofacial Dysostoses, MFD1,Mandibulofacial Dysostosis, MFD1,Syndrome, Franceschetti-Zwahlen-Klein,Syndrome, Treacher Collins,Syndrome, Treacher Collins-Franceschetti,Syndromes, Franceschetti-Zwahlen-Klein,Syndromes, Treacher Collins-Franceschetti,Treacher Collins Franceschetti Syndrome,Treacher Collins-Franceschetti Syndromes
D010641 Phenotype The outward appearance of the individual. It is the product of interactions between genes, and between the GENOTYPE and the environment. Phenotypes
D011859 Radiography Examination of any part of the body for diagnostic purposes by means of X-RAYS or GAMMA RAYS, recording the image on a sensitized surface (such as photographic film). Radiology, Diagnostic X-Ray,Roentgenography,X-Ray, Diagnostic,Diagnostic X-Ray,Diagnostic X-Ray Radiology,X-Ray Radiology, Diagnostic,Diagnostic X Ray,Diagnostic X Ray Radiology,Diagnostic X-Rays,Radiology, Diagnostic X Ray,X Ray Radiology, Diagnostic,X Ray, Diagnostic,X-Rays, Diagnostic
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D006053 Goldenhar Syndrome Mandibulofacial dysostosis with congenital eyelid dermoids. Hemifacial Microsomia,Oculoauriculovertebral Syndrome,Craniofacial Microsomia,Facioauriculovertebral Dysplasia,Facioauriculovertebral Sequence,First and Second Branchial Arch Syndrome,First and Second Pharyngeal Arch Syndromes,Goldenhar Disease,Goldenhar Syndrome with Ipsilateral Radial Defect,Goldenhar-Gorlin Syndrome,Hemifacial Microsomia with Radial Defects,Lateral Facial Dysplasia,Microsomia Hemifacial Radial Defects,Moeschler Clarren Syndrome,OAVS with Radial Defect,Oculoauriculovertebral Dysplasia,Oculoauriculovertebral Spectrum,Oculoauriculovertebral Spectrum with Radial Defect,Oral-Mandibular-Auricular Syndrome,Otomandibular Dysostosis,Craniofacial Microsomias,Dysostosis, Otomandibular,Dysplasia, Facioauriculovertebral,Dysplasia, Lateral Facial,Dysplasia, Oculoauriculovertebral,Dysplasias, Facioauriculovertebral,Dysplasias, Lateral Facial,Dysplasias, Oculoauriculovertebral,Facial Dysplasia, Lateral,Facial Dysplasias, Lateral,Facioauriculovertebral Dysplasias,Facioauriculovertebral Sequences,Goldenhar Gorlin Syndrome,Goldenhar-Gorlin Syndromes,Lateral Facial Dysplasias,Microsomia, Craniofacial,Microsomias, Craniofacial,Oculoauriculovertebral Dysplasias,Oculoauriculovertebral Spectrums,Oral Mandibular Auricular Syndrome,Oral-Mandibular-Auricular Syndromes
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults

Related Publications

A Medina Banegas, and M Gil Vélez, and J M Osete Albaladejo, and F Argudo Marco, and J Díaz-Yelo
January 1996, Revue de laryngologie - otologie - rhinologie,
A Medina Banegas, and M Gil Vélez, and J M Osete Albaladejo, and F Argudo Marco, and J Díaz-Yelo
January 1983, Annales de dermatologie et de venereologie,
A Medina Banegas, and M Gil Vélez, and J M Osete Albaladejo, and F Argudo Marco, and J Díaz-Yelo
June 1984, Klinika oczna,
A Medina Banegas, and M Gil Vélez, and J M Osete Albaladejo, and F Argudo Marco, and J Díaz-Yelo
January 2006, Journal of pediatric ophthalmology and strabismus,
A Medina Banegas, and M Gil Vélez, and J M Osete Albaladejo, and F Argudo Marco, and J Díaz-Yelo
January 1992, Journal francais d'ophtalmologie,
A Medina Banegas, and M Gil Vélez, and J M Osete Albaladejo, and F Argudo Marco, and J Díaz-Yelo
August 1992, Anales espanoles de pediatria,
A Medina Banegas, and M Gil Vélez, and J M Osete Albaladejo, and F Argudo Marco, and J Díaz-Yelo
July 1969, Annales medico-psychologiques,
A Medina Banegas, and M Gil Vélez, and J M Osete Albaladejo, and F Argudo Marco, and J Díaz-Yelo
July 1972, Archives des maladies du coeur et des vaisseaux,
A Medina Banegas, and M Gil Vélez, and J M Osete Albaladejo, and F Argudo Marco, and J Díaz-Yelo
January 1986, Annales d'oto-laryngologie et de chirurgie cervico faciale : bulletin de la Societe d'oto-laryngologie des hopitaux de Paris,
A Medina Banegas, and M Gil Vélez, and J M Osete Albaladejo, and F Argudo Marco, and J Díaz-Yelo
December 1978, Pediatrie,
Copied contents to your clipboard!