Proops R, Green S H
J Med Genet. 1981 Apr;18(2):101-4. doi: 10.1136/jmg.18.2.101.
A family is described in which three children have neuronal ceroid lipofuscinosis and two of them also have an arthropathy. Clinically the children have the late infantile form but pathological evidence shows the recognised overlap with the juvenile form. A fourth child with joint involvement but with normal skin biopsies is described. It is suggested that this family have a specific form of neuronal ceroid lipofuscinosis with arthropathy and that accumulation of metabolites in this storage disease may be age dependent.
描述了一个家庭,其中三个孩子患有神经元蜡样脂褐质沉积症,其中两个孩子还患有关节病。临床上,这些孩子表现为晚期婴儿型,但病理证据显示与青少年型存在公认的重叠。描述了第四个有关节受累但皮肤活检正常的孩子。提示该家庭患有伴有关节病的一种特殊形式的神经元蜡样脂褐质沉积症,并且这种贮积病中代谢产物的积累可能与年龄有关。