ABSTRACT
La artrogriposis múltiple congénita puede definirse como una displasia articular sistémica, caracterizada por rigidez articular en múltiples localizaciones de forma congénita. Se presenta un caso en el que se diagnosticó prenatalmente este signo clínico, que puede tener múltiples causas subyacentes.
Arthrogryposis multiplex congenita may be defined as a systemic articular dysplasia characterized by articular rigidity in a many locations of congenital origin. A case was presented in which this clinical sign was diagnosed at prenatal phase and it may have many underlying causes.
ABSTRACT
PURPOSE: To analyze congenital anomalies, especially musculoskeletal anomalies, in patients with VATER association. MATERIALS AND METHODS: Fifteen patients who were admitted to our hospital from Jan. 1990 to Dec. 1997, and with more than three of the major criteria of VATER association, were included in this study. Major criteria were vertebral anomalies, imperforated anus, tracheoesophageal anomalies, radial side anomalies, renal anomalies and congenital heart anomalies. RESULTS: Seven boys and 8 girls with VATER association were included. The follow-up period, except for 4 cases who died, was 6 years and 8 months on average (from 2 years and 3 months to 12 years and 7 months). Twelve patients had congenital heart disease, and 11 patients had tracheoesophageal anomalies and imperforated anus, 8 had vertebral anomalies, and radial side anomalies and renal anomalies were detected in 6 patients each. Congenital rib anomalies were the most common. CONCLUSION: Orthopedic surgeons who address vertebral or radial side anomalies in patients with VATER association need to predict other possible anomalies and should have enough knowledge to treat these conditions.