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title Genetic linkage of familial expansile osteolysis to chromosome 18q. | journal Hum. Mol. Genet. | volume 3 | issue 2 | pages 359–61
Kaynak: RANK

Although most hernias can be detected clinically with the presence of a lump with an expansile cough impulse some may be difficult to
Kaynak: Carnett's sign

On a radiograph, well-defined, expansile, lytic lesion is observed. Expansion of cortex gives the lesion a balloon-like appearance.
Kaynak: Aneurysmal bone cyst

Images usually show a sharply circumscribed but expansile mass. It may be difficult to exclude the intracranial connection if the defect
Kaynak: Nasal glial heterotopia

The lesion is usually identified as a well demarcated, expansile mass with an ossified rim at the periphery. Calcifications are noted
Kaynak: Juvenile active ossifying fibroma

They may be central, eccentric, expansile or nonexpansile. Differentiating an enchondroma from a bone infarct on plain film may be difficult
Kaynak: Enchondroma

Diagnosis: Non-expansile, non-ulcerative lesions. No involvement of viscera Osteolytic radiographic pattern. Negative hereditary, metabolic,
Kaynak: Gorham's disease

Osteolysis, familial expansile. 174810 TNFRSF11A Osteopathia striata with cranial sclerosis. 300373 FAM123B Osteopetrosis, AD type I
Kaynak: List of OMIM disorder codes

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