Inamadar Arun C, Palit Aparna
Department of Dermatology, Venereology and Leprosy, BLDEA's SBMP Medical College, Hospital and Research Centre, Bijapur, Karnataka, India.
Indian J Dermatol Venereol Leprol. 2007 Nov-Dec;73(6):417-9. doi: 10.4103/0378-6323.37063.
A 5-year-old boy was admitted for severe neurological impairment including hypotonia and loss of consciousness without preceding febrile illness. On examination, he had silver colored hair and bronze-tan over photo-exposed body parts. He was born of consanguineous parents and three of his elder siblings, who died in early childhood, had similar colored hair. Complete blood count and serum immunoglobulin levels were within normal limits. Peripheral blood smear did not show any cytoplasmic granules in neutrophils. Cerebro-spinal fluid examination did not reveal any abnormality. Light microscopic examination of the hair revealed irregular clumping of the melanin throughout the shafts. The patient died on the second day following admission. A clinical diagnosis of Elejalde disease was made. The clinical and genetic overlapping of the three silvery-hair syndromes has been discussed.
一名5岁男孩因严重神经功能障碍入院,包括肌张力减退和意识丧失,且无前驱发热性疾病。检查发现,他有银色头发,暴露于阳光下的身体部位呈青铜色。他的父母是近亲结婚,他的三个哥哥姐姐在幼儿期死亡,也有类似颜色的头发。全血细胞计数和血清免疫球蛋白水平在正常范围内。外周血涂片显示中性粒细胞无任何细胞质颗粒。脑脊液检查未发现任何异常。毛发的光镜检查显示整个毛干中黑色素不规则聚集。患者在入院后第二天死亡。做出了埃杰尔德病的临床诊断。讨论了三种银发综合征的临床和遗传重叠情况。