Judge M R, Shield J P, Cant A, Strobel S, Levin M, Reiser J, Harper J I
Department of Dermatology, Hospitals for Sick Children, London, U.K.
Br J Dermatol. 1991 Jun;124(6):606-8. doi: 10.1111/j.1365-2133.1991.tb04960.x.
The case is reported of a female infant, who at the age of 3 months developed severe erythroderma, marked hyperkeratosis of the palms and soles and subsequently extreme growth failure and intermittent diarrhoea. Her course was complicated by life-threatening infections but detailed investigation revealed no recognized underlying metabolic or immune abnormality.
报道了一名女婴的病例，该女婴在3个月大时出现严重的红皮病、手掌和足底明显的角化过度，随后出现极度生长发育迟缓及间歇性腹泻。她的病程因危及生命的感染而复杂化，但详细检查未发现公认的潜在代谢或免疫异常。
