Subject(s)
Humans , Male , Female , Adult , Middle Aged , Aged , Respiration, Artificial/adverse effects , Respiratory Muscles/pathology , Diaphragm/pathology , Muscle Weakness/diagnosis , Muscle Weakness/diagnostic imaging , Extremities/pathology , Muscles/pathology , Atrophy/diagnosis , Atrophy/diagnostic imaging , Prospective Studies , Ultrasonography , Critical Care , Intensive Care UnitsABSTRACT
Camurati-Engelmann disease (CED) is an autosomal dominant progressive diaphyseal dysplasia caused by mutations in the transforming growth factor-beta1 (TGFB1) gene. We report the first Korean family with an affected mother and son who were diagnosed with CED. The proband is a 19-yr-old male with a history of abnormal gait since the age of 2. He also suffered from proximal muscle weakness, pain in the extremities, and easy fatigability. Skeletal radiographs of the long bones revealed cortical, periosteal, and endosteal thickenings, predominantly affecting the diaphyses of the upper and lower extremities. No other bony abnormalities were noted in the skull and spine and no remarkable findings were seen on laboratory tests. The patient's mother had a long-standing history of mild limb pain. Under the impression of CED on radiographic studies, we performed mutation analysis. A heterozygous G to A transition at cDNA position +653 in exon 4 of the TGFB1 gene (R218H) was detected in the patient and his mother.