Like his brother Tim, Jon suffers from hereditary multiple exostoses.

It is associated with hereditary multiple exostoses.

Bone dysplasias, including Paget's disease, fibrous dysplasia, enchondromatosis, and hereditary multiple exostoses, increase the risk of osteosarcoma.

Hereditary multiple exostoses (HME)

Hereditary Multiple Exostoses (HME)

Hereditary multiple exostoses is inherited as an autosomal dominant genetic condition and is associated with abnormalities (mutations) in the EXT1 and EXT 2 genes.

PGD is also now being performed in a disease called Hereditary multiple exostoses (MHE/MO/HME).

Examples of this type of disorder are Huntington's disease, neurofibromatosis type 1, neurofibromatosis type 2, Marfan syndrome, hereditary nonpolyposis colorectal cancer, and hereditary multiple exostoses, which is a highly penetrant autosomal dominant disorder.

Hereditary multiple exostoses (HME or MHE), also known as Diaphyseal aclasis, is a rare medical condition in which multiple bony spurs or lumps (also known as exostoses, or osteochondromas) develop on the bones of a child.

Metachondromatosis demonstrates autosomal-dominant transmission and presents with both multiple osteochondromas and enchondromas.

Reichel's syndrome: Also known as synovial osteochondromatosis.

HME is synonymous with Multiple hereditary exostoses and Multiple osteochondromatosis, which is the preferred term used by the World Health Organization.

Synovial chondromatosis (synonyms include synovial osteochondromatosis, primary synovial osteochondromatosis, and synovial chondrometaplasia) is a disease affecting the synovium, a thin flexible membrane around a joint.

Synovial osteochondromatosis (SOC) (synonyms include synovial chondromatosis, primary synovial chondromatosis, synovial chondrometaplasia) is a rare disease that creates a benign change or proliferation in the synovium or joint-lining tissue, which changes to form bone-forming cartilage.

Like his brother Tim, Jon suffers from hereditary multiple exostoses.

It is associated with hereditary multiple exostoses.

Bone dysplasias, including Paget's disease, fibrous dysplasia, enchondromatosis, and hereditary multiple exostoses, increase the risk of osteosarcoma.

Hereditary multiple exostoses (HME)

Hereditary Multiple Exostoses (HME)

Hereditary multiple exostoses is inherited as an autosomal dominant genetic condition and is associated with abnormalities (mutations) in the EXT1 and EXT 2 genes.

PGD is also now being performed in a disease called Hereditary multiple exostoses (MHE/MO/HME).

Examples of this type of disorder are Huntington's disease, neurofibromatosis type 1, neurofibromatosis type 2, Marfan syndrome, hereditary nonpolyposis colorectal cancer, and hereditary multiple exostoses, which is a highly penetrant autosomal dominant disorder.

Hereditary multiple exostoses (HME or MHE), also known as Diaphyseal aclasis, is a rare medical condition in which multiple bony spurs or lumps (also known as exostoses, or osteochondromas) develop on the bones of a child.

Metachondromatosis demonstrates autosomal-dominant transmission and presents with both multiple osteochondromas and enchondromas.