Karrar Z A, Mabrouk A A
Department of Paediatrics, Faculty of Medicine, University of Khartoum, Sudan.
Ann Trop Paediatr. 1991;11(4):367-70. doi: 10.1080/02724936.1991.11747530.
This case report describes the rare variant of autosomal recessive cutis laxa with bone dystrophy in a Sudanese child. The clinical features include cutis laxa, growth and development retardation, facial dysmorphism, hyperextensible joints, dislocation of the hips and a large umbilical hernia.
本病例报告描述了一名苏丹儿童患有的伴有骨营养不良的常染色体隐性遗传性皮肤松弛症罕见变异型。临床特征包括皮肤松弛、生长发育迟缓、面部畸形、关节过度伸展、髋关节脱位和巨大脐疝。