Hereditary Multiple Exostosis (Diahyseal Aclasia)
Hereditary multiple exostosis, also known as diaphyseal aclasis, is a genetic condition often passed down to a child by one parent, but it can also be caused by a genetic mutation, meaning it can occur on its own by a change.
Osteochondroma & Multiple Hereditary Exostosis - Orthobullets
Osteochondromas are benign chondrogenic lesions derived from aberrant cartilage from the perichondral ring that may take the form of solitary osteochondroma, or Multiple Hereditary Exostosis. Patients typically present between the ages of 10 and 30 with a painless mass.
Hereditary multiple exostoses - Wikipedia
Hereditary multiple osteochondromas (HMO), also known as hereditary multiple exostoses, is a disorder characterized by the development of multiple benign osteocartilaginous masses (exostoses) in relation to the ends of long bones of the lower limbs such as the femurs and tibias and of the upper limbs such as the humeri and forearm bones.
Hereditary Multiple Osteochondromas (Multiple Hereditary Exostoses)
2022年7月5日 · Hereditary multiple osteochondromas (HMO) — sometimes called multiple hereditary exostoses — causes benign tumors to form along the bones and growth plates of children and adolescents. HMO is a lifelong condition that can cause pain and skeletal changes.
Hereditary Multiple Osteochondromas - GeneReviews® - NCBI Bookshelf
2000年8月3日 · Hereditary multiple osteochondromas (HMO), previously called hereditary multiple exostoses (HME), is characterized by growths of multiple osteochondromas, benign cartilage-capped bone tumors that grow outward from the metaphyses of long bones.
Hereditary Multiple Exostoses: a review of clinical appearance …
Hereditary multiple exostoses (HME) is an inherited genetic condition characterized by the presence of multiple exostoses (osteochondromas). MHE is a relatively rare autosomal dominant disorder, mainly caused by loss of function mutations in two genes: exostosin-1 (EXT1) and exostosin-2 (EXT2).
What Is Multiple Hereditary Exostosis? - WebMD
2024年9月4日 · Multiple hereditary exostosis is a rare genetic condition typically passed down from parent to child. A mutated gene can also cause the disease. If a parent has multiple...
Hereditary multiple exostoses: are there new plausible treatment ...
Hereditary multiple exostoses (HME) is a rare congenital pediatric disorder characterized by osteochondromas forming next to the growth plates in young patients. The osteochondromas cause multiple health problems that include skeletal deformities and chronic pain.
Hereditary multiple osteochondromas - MedlinePlus
Hereditary multiple osteochondromas is a condition in which people develop multiple benign (noncancerous) bone tumors called osteochondromas. The number of osteochondromas and the bones on which they are located vary greatly among affected individuals.
Hereditary multiple exostoses — Knowledge Hub - GeNotes
Hereditary multiple exostoses (HME), also known as hereditary multiple osteochondromas, is a rare bone condition characterised by multiple bony growths or osteochondromas (benign cartilage-capped bone tumours that grow outward from the metaphysis of long bones).