Najjar S S, Salem G M, Idriss Z H
Acta Paediatr Scand. 1975 Mar;64(2):273-9. doi: 10.1111/j.1651-2227.1975.tb03834.x.
Six patients with congenital generalized lipodystrophy are described. They had generalized paucity of fat tissue, acanthosis nigricans, prominent superficial veins and muscle hypertrophy. They were mentally retarded. Three had corneal opacities. They had normal external genitalia and none was tall for age. Their bone age was advanced and some had minor skeletal anomalies and nephromegaly. The muscle histology on light microscopy was normal. The majority had elevated serum aldolase and to a lesser degree serum lactic dehydrogenase and creatinine phosphokinase. Four of five examined had a myopathic electromyogram. They had normal or deranged liver function tests. The fatty liver infiltration in one seems to be progressive. Four had a normal and two an abnormal metyrapone test. They had an age-dependent abnormality of growth hormone, insulin and carbohydrate homeostasis.
本文描述了6例先天性全身脂肪营养不良患者。他们全身脂肪组织缺乏,有黑棘皮病、浅表静脉突出和肌肉肥大。他们存在智力发育迟缓。3例有角膜混浊。他们外生殖器正常,且身高均未超过同龄人。他们骨龄提前,部分有轻微骨骼异常和肾肿大。光镜下肌肉组织学正常。大多数患者血清醛缩酶升高,血清乳酸脱氢酶和肌酸磷酸激酶也有不同程度升高。5例接受检查的患者中有4例肌电图呈肌病表现。他们肝功能检查结果正常或异常。其中1例的脂肪肝浸润似乎在进展。4例甲吡酮试验结果正常,2例异常。他们存在与年龄相关的生长激素、胰岛素和碳水化合物稳态异常。