Beals R K, Bird C B
Birth Defects Orig Artic Ser. 1975;11(6):107-12.
A 19-year-old girl with carpal and tarsal osteolysis has been presented. The clinical course was characterized by normal early growth and motor development followed by the insidious onset in early childhood of a progressive, peripheral joint destruction, especially in the tarsal and carpal bones. The patient's course was complicated by acquired spasticity from platybasia, scoliosis, generalized muscle weakness, mild growth failure and corneal clouding.
本文报告了一名19岁患有腕骨和跗骨骨质溶解的女孩。其临床病程特点为早期生长和运动发育正常,随后在幼儿期隐匿起病,出现进行性外周关节破坏,尤其是跗骨和腕骨。患者的病程因扁平颅底导致的后天性痉挛、脊柱侧凸、全身肌肉无力、轻度生长发育迟缓以及角膜混浊而变得复杂。