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Hereditary multiple exostoses is a rare congenital condition with autosomal dominant inheritance. It consists of formation of osteocartilaginous exostoses, most commonly from the metaphysis of long bones. Surgery is the main treatment as there is no available medical treatment.
Emma Sønderskov +3 more
+4 more sources
Hereditary multiple exostoses is a rare congenital condition with autosomal dominant inheritance. It consists of formation of osteocartilaginous exostoses, most commonly from the metaphysis of long bones. Surgery is the main treatment as there is no available medical treatment.
Emma Sønderskov +3 more
+4 more sources
1980
The cause of hereditary multiple exostoses (synonyms: multiple osteocartilaginous exostoses, multiple osteochondromas, diaphyseal aclasis etc.) is a congenital developmental differentiation error of bone. Different opinions exist as to their pathogenesis (Bethge 1963; Solomon 1963; Cocchi 1952; Witt et al. 1966; a.o.).
Walter Blauth +1 more
openaire +1 more source
The cause of hereditary multiple exostoses (synonyms: multiple osteocartilaginous exostoses, multiple osteochondromas, diaphyseal aclasis etc.) is a congenital developmental differentiation error of bone. Different opinions exist as to their pathogenesis (Bethge 1963; Solomon 1963; Cocchi 1952; Witt et al. 1966; a.o.).
Walter Blauth +1 more
openaire +1 more source
1999
They are characterized by heredity, multiple and rather symmetrical distribution1, frequent limb-shortening and/or deformity, considerable incidence of secondary chondrosarcoma.
openaire +1 more source
They are characterized by heredity, multiple and rather symmetrical distribution1, frequent limb-shortening and/or deformity, considerable incidence of secondary chondrosarcoma.
openaire +1 more source
Genetic testing in prostate cancer management: Considerations informing primary care
Ca-A Cancer Journal for Clinicians, 2022Veda N Giri, Todd M Morgan, David Morris
exaly
Hereditary multiple exostoses. Hereditary multiple exostoses in horses.
The American journal of pathology, 1981J L, Shupe +3 more
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