Absence of the common crus in Goldenhar syndrome.
L Manfré, P Genuardi, M Tortorici… - American journal of …, 1997 - Am Soc Neuroradiology
We describe an unusual labyrinthine malformation in a case of Goldenhar syndrome studied
with CT and steady-state MR imaging. A single posterosuperior semicircular canal was …
with CT and steady-state MR imaging. A single posterosuperior semicircular canal was …
Unilateral semicircular canal aplasia in Goldenhar's syndrome
MM Lemmerling, BD Vanzieleghem… - American journal …, 2000 - Am Soc Neuroradiology
A patient with Goldenhar's syndrome (oculoauriculovertebral dysplasia) and unilateral
aplasia of all semicircular canals is presented. This is the first report of such a finding and …
aplasia of all semicircular canals is presented. This is the first report of such a finding and …
Goldenhar syndrome: associated with submandibular gland hyperplasia and hemihypoplasia of the mobile tongue
RT Miyamoto, RC Hamaker… - Archives of …, 1976 - jamanetwork.com
• We report a case of Goldenhar syndrome with submandibular gland hyperplasia and
hemihypoplasia of the mobile tongue. This association has not been noted in the literature …
hemihypoplasia of the mobile tongue. This association has not been noted in the literature …
[CITATION][C] Goldenhar association and cranial defects
RM Pauli, JH Jung… - American Journal of …, 1983 - Wiley Online Library
Wilson has summarized reported cases in which the Goldenhar anomaly was associated
with cranial and brain defects [Wilson, 19831; hydrocephalus was present in five of these …
with cranial and brain defects [Wilson, 19831; hydrocephalus was present in five of these …
Atypical goldenhar syndrome: a case report.
AK Jena, R Duggal - Journal of Clinical Pediatric Dentistry, 2006 - search.ebscohost.com
A patient with atypical Goldenhar syndrome is reported. The characteristic features similar to
the other reported cases are facial asymmetry, multiple skin tags, limbal dermoids and …
the other reported cases are facial asymmetry, multiple skin tags, limbal dermoids and …
The Goldenhar syndrome: a natural history.
MH Shokeir - Birth defects original article series, 1977 - europepmc.org
Twenty-four patients with the 1st branchial arch (Goldenhar) syndrome have been
ascertained ranging in age from newborn to 58 years. In infancy, the ocular, auricular, and …
ascertained ranging in age from newborn to 58 years. In infancy, the ocular, auricular, and …
Encephalocele (cerebellocele) in the Goldenhar-Gorlin syndrome
S Aleksic, G Budzilovich, MA Greco, F Epstein… - European Journal of …, 1983 - Springer
A patient with unilateral preauricular appendages and occipital mass is described who died
on the fifth day of life. An autopsy demonstrated congenital megabladder and megaureters …
on the fifth day of life. An autopsy demonstrated congenital megabladder and megaureters …
[CITATION][C] Laryngeal manifestations of Goldenhar syndrome
TM Andrews, SR Shott - American journal of otolaryngology, 1992 - Elsevier
1845.'Goldenhar,'in 1952, published clinical observations of the syndrome with the following
major findings:(1) epibulbar dermoids and/or lipodermoids,(2) auricular appendices and …
major findings:(1) epibulbar dermoids and/or lipodermoids,(2) auricular appendices and …
Goldenhar syndrome with external auditory canal stenosis complicated by canal cholesteatoma and first branchial cleft cyst
GC Barkdull, D Carvalho - International Journal of Pediatric …, 2007 - Elsevier
This report features a case of Goldenhar syndrome with congenital left facial nerve paralysis,
microtia and external auditory canal stenosis complicated by an external auditory canal …
microtia and external auditory canal stenosis complicated by an external auditory canal …
Progressive hearing loss in Goldenhar's syndrome
A Parving - Scandinavian Audiology, 1978 - Taylor & Francis
A family with Goldenhar's syndrome is presented. The pattern of inheritance is autosomal
dominant with incomplete penetrance. The mutant gene in question has variable phenotypic …
dominant with incomplete penetrance. The mutant gene in question has variable phenotypic …