| luxatio | <orthopaedics> The displacement of any part, more especially of a bone. Synonym: luxation. Origin: L. Locare = to place (18 Nov 1997) |
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| luxatio erecta | Subglenoid dislocation of the head of the humerus; the arm is raised and abducted and cannot be lowered. (05 Mar 2000) |
| luxatio perinealis | A condition in which the head of the femur is dislocated to the perineum. (05 Mar 2000) |
| articulatio coxae | The ball-and-socket synovial joint between the head of the femur and the acetabulum. Synonym: articulatio coxae, coxa, thigh joint. (05 Mar 2000) |
| malum coxae | <rheumatology> Disease of the hip joint. (05 Mar 2000) |
| malum coxae senile | <orthopaedics> Deformity of the head of the femur caused by ischemic damage. Synonym: senile hip disease. (05 Mar 2000) |
| retinaculum capsulae articularis coxae | One of several longitudinal folds of the articular capsule of the hip joint reflected onto the femoral neck deep to which the retinacular branches of the medial femoral circumflex artery pass to reach the femoral head. Synonym: retinaculum capsulae articularis coxae, Weitbrecht's fibres. (05 Mar 2000) |
| musculus triceps coxae | <anatomy> The obturator internus and superior and inferior gemellus muscles considered as one muscle, inserting via a single tendon into the greater trochanter of the femur. Synonym: musculus triceps coxae, triceps muscle of hip. (05 Mar 2000) |
| os coxae | A large flat bone formed by the fusion of the ilium, ischium, and pubis (in the adult), constituting the lateral half of the pelvis; it articulates with its fellow anteriorly, with the sacrum posteriorly, and with the femur laterally. Synonym: os coxae, coxa, coxal bone, innominate bone, os innominatum. (05 Mar 2000) |
| triceps coxae muscle | <anatomy> The obturator internus and superior and inferior gemellus muscles considered as one muscle, inserting via a single tendon into the greater trochanter of the femur. Synonym: musculus triceps coxae, triceps muscle of hip. (05 Mar 2000) |
| amaurosis congenita of Leber | An autosomal recessive cone-rod abiotrophy causing blindness or severely reduced vision at birth. (05 Mar 2000) |
| amyoplasia congenita | Limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse aetiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms exist, autosomal dominant, recessive, and X-linked. Synonym: amyoplasia congenita. (05 Mar 2000) |
| amyotonia congenita | Atonic pseudoparalysis of congenital origin (neither familial nor hereditary), observed especially in infants and characterised by absences of muscular tone only in muscles innervated by the spinal nerves. Synonym: congenital atonic pseudoparalysis, myatonia congenita, Oppenheim's disease, Oppenheim's syndrome. An indefinite term for a number of congenital neuromuscular disorders that cause generalised myotonia in young children, and that have a benign course (static or regressive). (05 Mar 2000) |
| aplasia cutis congenita | Congenital absence or deficiency of a localised area of skin, with the base of the defect covered by a thin translucent membrane; most often a single area near the vertex of the scalp, but may occur in other areas; underlying structures may also be affected; autosomal inheritance, either dominant or recessive. (05 Mar 2000) |
| arthrogryposis multiplex congenita | Limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse aetiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms exist, autosomal dominant, recessive, and X-linked. Synonym: amyoplasia congenita. (05 Mar 2000) |