Create issue ticket

282 Possible Causes for Cranial Hyperostosis

  • Hyperostosis Frontalis Interna

    In summary, symmetric cranial hyperostosis is a common entity, occurring in 15-20% of normal females between the ages of 40 and 60.[] Stewart: Localized cranial hyperostosis in insane. Journal of Neurology and Psychopathology, London, 1928, 8: 321. F. Morel: L'hyperostose frontale interne.[] Aggressive cranial vault decompression for cranial hyperostosis: technical case report of two cases . Oper Neurosur. 2005 ; 57 ( ONS Suppl 1 ): 212 . 6.[]

  • Leontiasis

    There is, however, a further type of cranial hyperostosis, which remains localised in skull and mandible, and shows no signs of being a generalised disease.[] View Article PubMed Google Scholar Viljoen DL, Versfeld GA, Losken W, Beighton P: Polyostotic fibrous dysplasia with cranial hyperostosis: new entity or most severe form of[]

  • Camurati-Engelmann Syndrome

    However, the skull hyperostosis is progressive, and cranial nerve compression often recurs. Corticosteroids may delay skull hyperostosis and cranial nerve impingement.[] Mocco JKomotar RJZacharia BEFeldstein NABruce JN Aggressive cranial vault decompression for cranial hyperostosis: technical case report of two cases.[] hyperostosis Cranial involvement in CED is milder & rarely results in frontal bossing & proptosis.[]

  • Oculodentodigital Dysplasia

    Cranial hyperostosis and broad tubular bones may be present.[] X-ray shows prominent mandible and cranial hyperostosis. Dental abnormalities include hypodontia, microdontia, dental caries and partial anodontia.[] X-ray skull showed cranial hyperostosis and bilateral, symmetrical widening of the ramus of mandible [Figure 7]. No intracranial calcification was seen.[]

  • Frontometaphyseal Dysplasia

    Prominent supraorbital ridges, radiologic evidence of cranial hyperostosis, and flared metaphyses are characteristic.[] Frontometaphyseal dysplasia is a syndrome that encompasses cranial hyperostosis, abnormal tubulation of cylindrical bones, and other skeletal and extraskeletal abnormalities[]

  • Schwartz-Lelek Syndrome

    hyperostosis , hepatomegaly and diabetes malformation syndrome, indicative to a specific set of signs, symptoms or other health indicators, associated with a health challenge[] hyperostosis hepatomegaly Short stature deafness neutrophil dysfunction Short stature dysmorphic face pelvic scapula dysplasia Short stature heart defect craniofacial anomalies[] […] polysyndactyly Short s [ edit ] Short stature abnormal skin pigmentation mental retardation Short stature Brussels type Short stature contractures hypotonia Short stature cranial[]

  • Van Buchem Disease

    […] alkaline phosphatase Cranial hyperostosis Cranial nerve paralysis Optic atrophy from cranial nerve compression Increased bone mineral density • • • More clinical features[] , genetic Phenotypes Autosomal recessive inheritance ; Cranial hyperostosis ; Cranial nerve paralysis ; Elevated alkaline phosphatase ; Headache ; Hearing impairment ; Increased[] SOST gene, 17q21.31 (OMIM gene/locus number #60574 0 ) Phenotype Progressive skeletal overgrowth (especially skull) and cortical thickening and generalized osteosclerosis, cranial[]

  • Entrapment Neuropathy

    With the exception of objective hearing impairment, no other significant cranial neuropathy has been detected thus far.[] On reviewing the published literature, this case was found to be the first in which hyperostosis due to congenital anemia resulted in symptomatic entrapment neuropathy of[]

  • Macrocephaly

    Pathologic macrocephaly may be due to megalencephaly (enlarged brain), hydrocephalus (water on the brain), cranial hyperostosis (bone overgrowth), and other conditions.[] Causes include hydrocephalus, enlarged brain, and cranial hyperostosis.[]

  • Meningitis

    Herein, we report the clinical and histopathological features of a rare case of IgG4-related intracranial hypertrophic pachymeningitis involving cranial hyperostosis.[] […] related intracranial hypertrophic pachymeningitis involving cranial hyperostosis.[] Diagnosis of SAPHO syndrome Synovitis-acne-pustulosis-hyperostosis-osteitis (SAPHO) syndrome is characterized by multifocal aseptic osteomyelitis of an uncertain etiology.[]

Further symptoms

Similar symptoms