Sharawat Indar K, Dawman Lesa, Panda Prateek K
Pediatric Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
Department of Pediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
J Pediatr Neurosci. 2020 Jul-Sep;15(3):332-333. doi: 10.4103/jpn.JPN_6_20. Epub 2020 Nov 6.
Late infantile metachromatic leukodystrophy is an autosomal recessive disorder caused by a deficiency in the enzyme activity of Aryl sulfatase-A. The classical presentation is characterized by gait disturbance, frequent fall, toe walking, impaired swallowing and feeding, seizures, progressive neuroregression, decorticate posture and early death. Here we report a toddler who presented with frequent falls and cognitive regression. Magnetic resonance imaging (MRI) showed a striking leopard skin pattern. Recognition of this pattern on MRI in proper clinical context can serve as a clue to the diagnosis.
晚期婴儿型异染性脑白质营养不良是一种常染色体隐性疾病,由芳基硫酸酯酶-A的酶活性缺乏引起。典型表现为步态障碍、频繁跌倒、足尖行走、吞咽和进食受损、癫痫发作、进行性神经退化、去皮质姿势及早期死亡。在此,我们报告一名出现频繁跌倒和认知退化的幼儿。磁共振成像(MRI)显示出显著的豹皮样图案。在恰当的临床背景下,识别MRI上的这种图案可作为诊断线索。