منابع مشابه
Infantile coxa vara.
Infantile or developmental coxa vara is a relatively infrequent localised dysplasia of unknown etiology which usually presents in the second or third year of life soon after the child begins walking. The clinical and radiological picture is usually characteristic especially when seen early. Early surgery leads to a satisfactory outcome. However, difficulty arises in diagnosis and treatment when...
متن کاملFamilial infantile coxa vara.
Case 1-A man of thirty-six sought advice because he had wrenched his left hip while cycling. He had had previous trouble with his hips from the age of eighteen, but the attacks of pain were infrequent and settled rapidly. He worked as a brewery manager with little difficulty. Four years before he attended he had had a piece of bone removed from the right knee for osteochondritis. Figure 1 shows...
متن کاملObservations on infantile coxa vara.
In 1907 Elmslie suggested that in some cases of congenital coxa vara without other abnormalities injury at birth might perhaps be one factor. He described accurately the cervical breach in infantile coxa vara with the typical metaphysial wedge included in the proximal fragment, and pointed out that there was often a clear history of injury. In 1913 he described thirty-four cases of the infantil...
متن کاملCACP syndrome (Camptodactyly Arthropathy Coxa Vara Pericarditis). Clinical case
Case Report Our patient, a 6 year old girl was diagnosed with the CACP syndrome at the age of 30 months. Her parents were negative for consanguinity. As an infant the patient was diagnosed with camptodactyly. At the age of 18 months frequent swelling of the knee was observed. Examination by rheumatologist confirmed the presence of swelling to elbows, wrists, knees, and ankles, without limitatio...
متن کاملCamptodactyly, Arthropathy, Coxa vara, Pericarditis (CACP)Syndrome: A Case Report
The camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is characterized by congenital or early-onset camptodactyly, childhood-onset noninflammatory arthropathy associated with synovial hyperplasia. Some patients have progressive coxa vara deformity and/or noninflammatory pericardial effusion. CACP is inherited as an autosomal recessive mode and the disease gene is assigned to a 1....
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1930
ISSN: 0035-9157
DOI: 10.1177/003591573002400114