A cutaneous lesion usually serves as a portal of entry for the infection, but sometimes no such lesion is found. They normally resolve, but tend to leave depressions in the skin. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. A subacute or chronic inflammatory disease of muscle and skin, marked by proximal muscle weakness and a characteristic skin rash. A bad taste in the mouth. A developmental deformity of the occipital bone and upper end of the cervical spine, in which the latter appears to have pushed the floor of the occipital bone upward.
Dermatomyositis may occur in association with malignant neoplasms. A disease marked by repeated episodes of increased bone resorption followed by excessive attempts at repair, resulting in weakened, deformed bones of increased mass. A condition characterized by shortness of the neck resulting from reduction in the number of vertebrae or the fusion of multiple hemivertebrae into one osseous mass. A developmental deformity of the occipital bone and upper end of the cervical spine, in which the latter appears to have pushed the floor of the occipital bone upward. Presyncope refers to the sensation of lightheadedness and loss of strength that precedes a syncopal event or accompanies an incomplete syncope. It is characterized by inflammation and degeneration of cartilage and can result in deformities such as floppy ear and saddle nose. The condition is most often seen in women, alone or in association with other disorders. A condition characterized by pain in or near the lateral humeral epicondyle or in the forearm extensor muscle mass as a result of unusual strain. The disease is associated with a complement mediated intramuscular microangiopathy, leading to loss of capillaries, muscle ischemia, muscle-fiber necrosis, and perifascicular atrophy. A condition characterized by alterations of the sense of taste which may range from mild to severe, including gross distortions of taste quality. The most common manifestations of Ehlers-Danlos Syndrome are hyperextensible skin and joints, skin fragility and reduced wound healing capability. A change from the patient's baseline sleeping pattern, either an increase or a decrease in the number of hours slept. The illness occurs with approximately equal frequency in children and adults. Osteoporosis is classified as primary Type 1, postmenopausal osteoporosis; Type 2, age-associated osteoporosis; and idiopathic, which can affect juveniles, premenopausal women, and middle-aged men and secondary osteoporosis which results from an identifiable cause of bone mass loss. The hairline is low and the motion of the neck is limited. Syndactylies are classified as complete or incomplete by the degree of joining. A subacute or chronic inflammatory disease of muscle and skin, marked by proximal muscle weakness and a characteristic skin rash. A complex systemic syndrome with inflammatory and autoimmune components that affect the skin, fascia, muscle, nerve, blood vessels, lung, and heart. Affected individuals exhibit short stature caused by rhizomelic shortening of the limbs, characteristic facies with frontal bossing and mid-face hypoplasia, exaggerated lumbar lordosis, limitation of elbow extension, genu varum, and trident hand. Syndactylies can also be simple or complex. A congenital anomaly of the hand or foot, marked by the webbing between adjacent fingers or toes. A condition that is characterized by a decrease in bone mass and density, causing bones to become fragile. This condition is most often precipitated by trauma to soft tissue or nerve complexes. This condition is associated with unstable depolarization of axonal membranes, primarily in the peripheral nervous system. A broken bone caused by disease, often by the spread of cancer to the bone.
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