Fichtel Jill C, Richards Judith A, Davis Loretta S
Section on Dermatology, Department of Medicine, The Medical College of Georgia, 1004 Chafee Avenue, Augusta, GA 30904, USA.
Pediatr Dermatol. 2007 Jan-Feb;24(1):25-7. doi: 10.1111/j.1525-1470.2007.00327.x.
Argininosuccinicaciduria is a rare metabolic disorder of the urea cycle associated with the inability to excrete nitrogenous waste in the form of urea. Along with low serum arginine, hepatomegaly, and mental retardation, congenital trichorrhexis nodosa is a distinguishing feature of the disorder. We present a 3.5-year-old girl diagnosed with argininosuccinicaciduria who presented to the dermatology clinic with hair thinning and loss since birth. Microscopic evaluation revealed nodular swellings on the hair shafts and frayed cortical fibers consistent with the diagnosis of trichorrhexis nodosa occurring in the setting of argininosuccinicaciduria.
精氨琥珀酸尿症是一种罕见的尿素循环代谢紊乱疾病,与无法以尿素形式排泄含氮废物有关。除了血清精氨酸水平低、肝肿大和智力迟钝外,先天性结节性脆发症是该疾病的一个显著特征。我们报告一名3.5岁被诊断为精氨琥珀酸尿症的女孩,自出生以来头发就逐渐稀疏并脱落,她到皮肤科诊所就诊。显微镜检查显示毛干上有结节状肿胀以及皮质纤维磨损,这与在精氨琥珀酸尿症背景下发生的结节性脆发症诊断相符。