OSLAM syndrome | |
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Other names | Osteosarcoma-limb anomalies-erythroid macrocytosis syndrome |
![]() | |
OSLAM syndrome is inherited in an autosomal dominant manner | |
Deaths | idk |
OSLAM syndrome is a rare autosomal dominant hereditary disorder. Its name is an initialism of " osteosarcoma, limb anomalies, and erythroid macrocytosis with megaloblastic marrow syndrome". OSLAM syndrome was recognised and described by Mulvilhill et al. as a syndrome that increases susceptibility to tumours and is characterised by an impaired regulation of bone and marrow development. [1] [2]
Individuals with OSLAM syndrome have an elevated risk of bone cancer, limb abnormalities, and enlarged red blood cells.
Clinical presentation is consistent with:[ citation needed]
![]() | This section is empty. You can help by
adding to it. (August 2017) |
![]() | This section is empty. You can help by
adding to it. (August 2017) |
OSLAM syndrome | |
---|---|
Other names | Osteosarcoma-limb anomalies-erythroid macrocytosis syndrome |
![]() | |
OSLAM syndrome is inherited in an autosomal dominant manner | |
Deaths | idk |
OSLAM syndrome is a rare autosomal dominant hereditary disorder. Its name is an initialism of " osteosarcoma, limb anomalies, and erythroid macrocytosis with megaloblastic marrow syndrome". OSLAM syndrome was recognised and described by Mulvilhill et al. as a syndrome that increases susceptibility to tumours and is characterised by an impaired regulation of bone and marrow development. [1] [2]
Individuals with OSLAM syndrome have an elevated risk of bone cancer, limb abnormalities, and enlarged red blood cells.
Clinical presentation is consistent with:[ citation needed]
![]() | This section is empty. You can help by
adding to it. (August 2017) |
![]() | This section is empty. You can help by
adding to it. (August 2017) |