A father and daughter both had multiple pathological fractures and nodal osteoarthropathy. The father, aged 50 years, had at least 20 healed fractures of the axial and appendicular skeleton, sustained by minor trauma over his 50-year lifespan, many of which had been surgically fixed prior to his first presentation to us. Fractures of the clavicles, thoracic cage and long bones of the arms and legs, had healed with malalignment and deformity. Healed fractures were complicated by ankylosis of the cervical vertebrae and both elbows. He also had osteoarthritis of the hands, with exuberant osteophytosis, and profound perceptive deafness. His general health was good, his intellect and facies were normal, and his sclerae were white. The daughter, ...
The Piepkorn type of lethal osteochondrodysplasia (POCD) is a rare and lethal dwarfing condition. Fo...
Hereditary multiple exostoses is an autosomal dominant disease with abnormal bone formation especial...
We report a large inbred kindred from Oman with a distinct type of spondyloepiphyseal dysplasia (SED...
SUMMARY A father and son, both affected by a skeletal dysplasia with severe craniofacial deform-itie...
We report on a father and his 4-year-old son sharing a characteristic dysmorphic facial phenotype (i...
We report 40 cases in one family of an autosomal dominant bone dysplasia, which, though similar in s...
We report two sibs, the ninth and tenth cases of a distinctive familial skeletal dysplasia. Designat...
Frontometaphyseal dysplasia is a rare genetic syndrome affecting the skeletal system and connective ...
Item does not contain fulltextFrontometaphyseal dysplasia is a rare genetic syndrome affecting the s...
Bone fragility is a pathological condition caused by altered homeostasis of the mineralized bone mas...
Background: Skeletal dysplasia's cause significant neurological symptoms and disrupt the development...
We report on an unusual family with an autosomal dominant limb-girdle type of myopathy and bone frag...
The skeletal dysplasias form a large group of hereditary disorders characterized by abnormal growth ...
Recent developments in tissue culture and enzyme analysis have made it possible to classify more pre...
textabstractMultiple epiphyseal dysplasia (MED) is one of the most common osteochondrodysplasias [Wy...
The Piepkorn type of lethal osteochondrodysplasia (POCD) is a rare and lethal dwarfing condition. Fo...
Hereditary multiple exostoses is an autosomal dominant disease with abnormal bone formation especial...
We report a large inbred kindred from Oman with a distinct type of spondyloepiphyseal dysplasia (SED...
SUMMARY A father and son, both affected by a skeletal dysplasia with severe craniofacial deform-itie...
We report on a father and his 4-year-old son sharing a characteristic dysmorphic facial phenotype (i...
We report 40 cases in one family of an autosomal dominant bone dysplasia, which, though similar in s...
We report two sibs, the ninth and tenth cases of a distinctive familial skeletal dysplasia. Designat...
Frontometaphyseal dysplasia is a rare genetic syndrome affecting the skeletal system and connective ...
Item does not contain fulltextFrontometaphyseal dysplasia is a rare genetic syndrome affecting the s...
Bone fragility is a pathological condition caused by altered homeostasis of the mineralized bone mas...
Background: Skeletal dysplasia's cause significant neurological symptoms and disrupt the development...
We report on an unusual family with an autosomal dominant limb-girdle type of myopathy and bone frag...
The skeletal dysplasias form a large group of hereditary disorders characterized by abnormal growth ...
Recent developments in tissue culture and enzyme analysis have made it possible to classify more pre...
textabstractMultiple epiphyseal dysplasia (MED) is one of the most common osteochondrodysplasias [Wy...
The Piepkorn type of lethal osteochondrodysplasia (POCD) is a rare and lethal dwarfing condition. Fo...
Hereditary multiple exostoses is an autosomal dominant disease with abnormal bone formation especial...
We report a large inbred kindred from Oman with a distinct type of spondyloepiphyseal dysplasia (SED...