Goldenhar Syndrome (Syndrome, Oculoauriculovertebral)

07/01/2014 - "Here we have described the case of a 10 years old girl had ocular, auricular & vertebral changes consistent with Goldenhar syndrome, she was managed with multidisciplinary approach and she was symptomatically improved but corrective surgery was planned as schedule of respective department. "

01/01/2004 - "To review the association of autism spectrum disorder (ASD) in individuals manifesting thalidomide embryopathy and Möbius sequence and compare them with three new studies in which ASD was also associated with ocular and systemic malformations: (1) a Swedish study of individuals with CHARGE association (Coloboma, Heart, choanal Atresia, developmental or growth Retardation, Genital anomaly, and Ear involvement); (2) a Swedish study of Goldenhar syndrome; and (3) Brazilian Möbius syndrome (sequence) study. "
04/01/2005 - "These investigations include two associated with teratogens (thalidomide embryopathy, Mobius sequence with misoprostol) and three (most Mobius sequence cases, CHARGE association, Goldenhar syndrome) with no known etiology. "

11/01/1996 - "Typical manifestations of both the Goldenhar syndrome and the caudal regression syndrome are present in this complex. "
01/01/1991 - "The authors study a case of sirenomelia at a 37 years old adult woman, nosographic table presented for the first time by Charles Duhamel in 1959, having the denomination of "caudal regression syndrome", similar to Goldenhar syndrome cephalic expression of this regression. "

01/01/2013 - "Oculoauriculovertebral spectrum (OAVS) or Goldenhar syndrome is a wide spectrum of congenital anomalies that involves structures arising from the first and second branchial arches. "
07/01/2009 - "Treatment of otological features of the oculoauriculovertebral dysplasia (Goldenhar syndrome)."
03/01/2009 - "Familial transmission of oculoauriculovertebral spectrum (Goldenhar syndrome) is not due to mutations in either EYA1 or SALL1."
01/01/2007 - "31 cases with oculoauriculovertebral dysplasia (Goldenhar syndrome): clinical, neuroradiologic, audiologic and cytogenetic findings."
05/01/2006 - "Goldenhar syndrome (oculoauriculovertebral dysplasia): report of one case."

05/01/2013 - "Methods :  We obtained a series of two-dimensional and three-dimensional images of 50 participants, aged 0-20 years, diagnosed with craniofacial microsomia, microtia, or Goldenhar syndrome. "
12/01/2007 - "Goldenhar syndrome is a well-known condition featuring the following triad of anomalies: ocular abnormalities, microtia and vertebral anomalies. "
04/01/2005 - "We also present two rare cases of bilateral Goldenhar syndrome and familial microtia with meatal atresia, respectively, in whom we also excluded TCOF1 mutations. "
04/01/2005 - "Exclusion of TCOF1 mutations in a case of bilateral Goldenhar syndrome and one familial case of microtia with meatal atresia."
03/01/2015 - "Hemifacial microsomia, cranial asymmetry, multiple ear tags, skin tags around the mouth and microtia were the most prominent facial features encountered in six patients with Goldenhar syndrome. "

11/01/2007 - "Seventeen children (mean age 7.6 years) with various syndromes (hemifacial/craniofacial microsomia, Goldenhar syndrome, Treacher Collins syndrome, Nager syndrome and Pyle-Bakwin-Krida syndrome) participated. "
07/01/2007 - "Patient diagnoses included unilateral craniofacial microsomia (n = 2), bilateral craniofacial microsomia (n = 3), Goldenhar syndrome (n = 1), Nager syndrome (n = 1), and Treacher-Collins syndrome (n = 1). "
12/01/2002 - "Conditions discussed include craniofacial microsomia, Goldenhar syndrome, Treacher Collins syndrome, Nager syndrome, Binder syndrome, and Pierre Robin sequence. "
04/01/2005 - "A number of different disorders involving first and second branchial arch anomalies have been described as distinct entities, including Treacher-Collins-Franceschetti syndrome, Goldenhar syndrome, Nager syndrome and Miller syndrome. "
10/01/2012 - "Monogenic syndromes were identified in 6% (12/204) of CL±P cases: Van der Woude syndrome (2 cases); CHARGE syndrome (2 cases); ectrodactyly, ectodermal dysplasia, and cleft/lip palate (EEC) syndrome (2 cases); branchiooculofacial (BOF) syndrome (1 case); Treacher-Collins syndrome (1 case); Nager syndrome (1 case); Goldenhar syndrome (1 case); holoprosencephaly spectrum (1 case); and Meckel syndrome (1 case). "

11/01/1993 - "Some of these clinical signs are present both in the Goldenhar syndrome and in the Townes-Brocks syndrome."
11/01/1993 - "Description of a patient with difficult nosological classification: Goldenhar syndrome or Townes-Brocks syndrome?"
05/15/2007 - "We report on wide phenotypic variations within a family with SALL1 mutations; the elder sister presented with a Townes-Brocks syndrome phenotype including external ear anomalies, preaxial polydactyly, and anteriorly placed anus, whereas the younger sister presented with a phenotype resembling Goldenhar syndrome, including atretic ear canals, mandibular hypoplasia, and right preaxial polydactyly as well as an epibulbar dermoid. "
12/01/2014 - "It has been shown to be associated with Goldenhar syndrome, Townes-Brocks syndrome, Treacher-Collins syndrome, VACTERL syndrome, and Wolf-Hirschhron syndrome. "

01/01/2008 - "Goldenhar syndrome associated with growth hormone deficiency."
06/01/1993 - "We have experienced the case of a 10-year-old boy who had Goldenhar syndrome accompanied by growth hormone (GH) deficiency. "
06/01/1993 - "A case of Goldenhar syndrome associated with growth hormone deficiency."
06/01/1993 - "We found no untoward effects of the hormone and we consider that treatment with GH is useful for patients who present with Goldenhar syndrome associated with growth hormone deficiency."

05/01/2009 - "Systemic associations included Goldenhar syndrome and Treacher-Collins-Franceschetti syndrome. "
04/01/2005 - "After the identification of mutations in TCOF1 as a general cause of the Treacher-Collins-Franceschetti syndrome, TCOF1 mutations were excluded in patients with unilateral signs of the Goldenhar syndrome spectrum. "
04/01/2005 - "A number of different disorders involving first and second branchial arch anomalies have been described as distinct entities, including Treacher-Collins-Franceschetti syndrome, Goldenhar syndrome, Nager syndrome and Miller syndrome. "

08/01/2007 - "Of the rest, 3 had a cordocentesis with normal chromosome fragility tests (VACTERL association, Goldenhar syndrome and Acrofacial dysostosis) and 4 declined testing (2 TOP with Cornelia de Lange, 2 ongoing pregnancies diagnosed postpartum with Fanconi anaemia and VACTERL association). "
12/01/2014 - "It has been shown to be associated with Goldenhar syndrome, Townes-Brocks syndrome, Treacher-Collins syndrome, VACTERL syndrome, and Wolf-Hirschhron syndrome. "

01/01/2015 - "Novel airway management in a child with Goldenhar Syndrome at a remote location."
04/01/2012 - "Airway management using the ProSeal laryngeal mask airway in a child with Goldenhar syndrome."
07/01/2011 - "Successful airway management in a patient with Goldenhar syndrome using preoperative three-dimensional computed tomography."
05/01/2008 - "Children with Goldenhar syndrome are known to present airway management challenges for the anesthesiologist. "
05/01/2008 - "Airway management in a patient with Goldenhar syndrome: a case report."

05/01/2011 - "The cases of 4 patients who underwent free-flap reconstruction of a severely hypoplastic mandible due to Goldenhar syndrome are presented. "
05/01/2011 - "Microvascular free flaps for mandibular reconstruction in Goldenhar syndrome."
07/01/1979 - "Surgical techniques using microvascular anastomoses and free flap transfers can now be applied in the management of patients with such conditions as Romberg disease, postirradiation hypoplasia of the face, and Goldenhar syndrome, and in patients with bronchial arch developmental defects. "

12/01/2006 - "We report a case of problematic tracheostomy placement in a 24-week-old ex-premature infant with Goldenhar syndrome. "
05/01/2012 - "Airway management for rigid bronchoscopy via a freshly performed tracheostomy in a child with Goldenhar syndrome."
12/01/2006 - "Tracheostomy is required in approximately 22% of children with Goldenhar syndrome because of upper airway obstruction. "

07/01/2015 - "Chin Wing Osteotomy for Bilateral Goldenhar Syndrome Treated by "Chin Wing Mentoplasty": Aesthetic, Functional, and Histological Considerations."
11/01/2002 - "The following report describes an unusual occurrence of a maxillary artery pseudoaneurysm following a Le Fort I and bilateral sagittal-split osteotomies for correction of mandibular and maxillary asymmetries in a patient with Goldenhar syndrome. "

06/01/2005 - "General anesthesia for a child with Goldenhar syndrome."
12/01/1994 - "[Fiberscopic intubation under general anesthesia for children with Goldenhar syndrome]."