Standard variant venous dysplasia of the cerebellum in a patient suffering from Muenke's syndrome and tinnitus

Auris Nasus Larynx

Volumn 28, Issue 3, 2001, Pages 249-252

  Dunne A A ^a   Bien, S ^a   Folz, B J ^a   Werner, J A ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

Coronal craniosynostosis; Muenke syndrome; Tinnitus; Venous dysplasia

Indexed keywords

ADULT; ARTICLE; AUDIOMETRY; BONE DYSPLASIA; BONE MALFORMATION; BRACHYDACTYLY; CARPAL BONE; CASE REPORT; CEREBELLUM; CLINICAL FEATURE; CRANIOFACIAL SYNOSTOSIS; DIAGNOSTIC TEST; HUMAN; MALE; MUENKE SYNDROME; PERCEPTION DEAFNESS; PETROUS BONE; TARSAL BONE; TINNITUS; VEIN MALFORMATION;

ADOLESCENT; ANGIOGRAPHY; AUDIOMETRY, PURE-TONE; CEREBELLUM; CEREBRAL VEINS; CRANIOSYNOSTOSES; HEARING LOSS, SENSORINEURAL; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; PETROUS BONE; SEVERITY OF ILLNESS INDEX; SYNDROME; TARSAL BONES; TINNITUS;

EID: 0034904390     PISSN: 03858146     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0385-8146(01)00054-2     Document Type: Article

References (7)

1. FGFR2 mutations in Peiffer Syndrome
2. Fibroblast growth factor receptor mutations in human skeletal disorders
3. Syndromes with craniosynostosis
4. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes
5. Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to pro250arg mutation in FGFR 3 gene
6. A unique mutation in fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
7. Stand der kontroversen diskussion um die pathogenese und behandlung des chronischen paukenergusses im kindesalter