Phenotypic manifestations and management of hyperostosis cranialis interna, a hereditary bone dysplasia affecting the calvaria and the skull base

American Journal of Medical Genetics, Part A

Volumn 152, Issue 3, 2010, Pages 547-555

  Waterval, J J ^a   Stokroos, R J ^a   Bauer, N J C ^a   De Bondt, R B J ^b   Manni, J J ^a  

^a MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

^b ISALA HOSPITAL   (Netherlands)

Author keywords

Cranial nerve disorder; Genetic; Hyperostosis; Osteochondrodysplasias; Osteosclerosis; Skull; Skull base

Indexed keywords

ANAMNESIS; ANOSMIA; ARNOLD CHIARI MALFORMATION; ARTICLE; AUDIOMETRY; BONE DYSPLASIA; CALVARIA; CLINICAL ARTICLE; DECOMPRESSION SURGERY; DIAGNOSTIC IMAGING; DISEASE COURSE; EPIPHORA; FACIAL NERVE DISEASE; FACIAL NERVE PARALYSIS; FEMALE; GENETIC COUNSELING; HEADACHE; HIGH RISK POPULATION; HUMAN; HYPEROSTOSIS; HYPEROSTOSIS CRANIALIS INTERNA; HYPOSMIA; MALE; PAPILLEDEMA; PERCEPTION DEAFNESS; PHENOTYPE; PRIORITY JOURNAL; SCLEROSIS; SKULL BASE; TINNITUS; TRIGEMINUS NEURALGIA; VESTIBULOCOCHLEAR NERVE DISEASE;

ADOLESCENT; ADULT; AGED; CHILD; DECOMPRESSION, SURGICAL; DIAGNOSIS, DIFFERENTIAL; FACIAL PARALYSIS; FEMALE; GENES, DOMINANT; HUMANS; HYPEROSTOSIS; MALE; MIDDLE AGED; NETHERLANDS; OSTEOSCLEROSIS; PEDIGREE; PHENOTYPE; SEX CHARACTERISTICS; SKULL; SKULL BASE; TOMOGRAPHY, X-RAY COMPUTED; YOUNG ADULT;

EID: 77649202021     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33205     Document Type: Article

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