GTS5:Enchondromatosis (IDH1, IDH2): Difference between revisions
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==Related Terminology== | ==Related Terminology== | ||
{| class="wikitable" | {| class="wikitable" | ||
|+ | |+ | ||
|Acceptable | |Acceptable | ||
| | |N/A | ||
|- | |- | ||
|Not Recommended | |Not Recommended | ||
| | |N/A | ||
|} | |} | ||
Ollier diseaseAcceptable: dyschondroplasia; multiple cartilaginous enchondromatosis; enchondromatosis Spranger type I, multiple enchondromas. | |||
Maffucci syndromeAcceptable: dyschondroplasia with haemangiomas; enchondromatosis with multiple cavernous haemangiomas; Kast syndrome; haemangiomatosis chondrodystrophica; enchondromatosis Spranger type II. | |||
==Definition/Description of Disease== | ==Definition/Description of Disease== | ||