Ip Patrick, Knight Ravi, Dokal Inderjeet, Manzur Adnan Y, Muntoni Francesco
Dubowitz Neuromuscular Centre, Department of Paediatrics and Neonatal Medicine, Imperial College London, Hammersmith Hospital, Du Cane Road, London W12 0NN, UK.
Eur J Paediatr Neurol. 2005;9(2):85-9. doi: 10.1016/j.ejpn.2005.01.007.
We report the case of a 3.5-year-old boy who presented with truncal ataxia, microcephaly and delayed global development in infancy. Hypoplasia of cerebellum and corpus callosum and delayed myelination were found on brain MRI. Failure to thrive, sparse hairs and dystrophic nails became evident at the age of 2 years. He subsequently developed bleeding tendency, thrombocytopenia and hypocellularity on bone marrow examination leading to a diagnosis of dyskeratosis congenita. Impaired pain perception with slowing of nerve conduction velocities was demonstrated, suggesting a mild peripheral neuropathy. To the best of our knowledge, peripheral neuropathy has never been reported as a feature of the congenital form of dyskeratosis congenita.
我们报告了一名3.5岁男孩的病例,该男孩在婴儿期出现躯干共济失调、小头畸形和整体发育迟缓。脑部MRI显示小脑和胼胝体发育不全以及髓鞘形成延迟。2岁时出现生长发育迟缓、毛发稀疏和指甲营养不良。随后,他出现出血倾向、血小板减少和骨髓检查显示细胞减少,最终诊断为先天性角化不良。同时还发现疼痛感知受损且神经传导速度减慢,提示存在轻度周围神经病变。据我们所知,周围神经病变从未被报道为先天性角化不良的特征。