Neurology Department, APHP, CHU de Bicêtre, Le Kremlin-Bicêtre, 78 rue du Général Leclerc, 94276, Kremlin-Bicêtre Cedex, France.
French National Reference Center for Rare Neuropathies (NNERF), 94276, Le Kremlin-Bicêtre, France.
Neurogenetics. 2021 Oct;22(4):333-341. doi: 10.1007/s10048-021-00668-z. Epub 2021 Aug 17.
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disease resulting from mutations in the NTRK1 gene encoding the neurotrophic tyrosine kinase-1 receptor. In this multicenter observational retrospective study, we investigated CIPA patients identified from French laboratories sequencing the NTRK1 gene, and seven patients were identified. Patients originated from France (2), Suriname (2), Mali (1), Kazakhstan (1), and Algeria (1). Mean age of patients was 9.8 years (4-20), four patients were female (57%), infant developmental milestones were delayed in four cases (57%), and four patients had a family history of consanguinity (57%). Mean age at diagnosis was 4.8 months (3-6), and all patients presented with pain insensitivity, anhidrosis, intellectual disability, self-mutilation, febrile episodes, impaired temperature perception, and autonomous nervous system impairment. Patients also showed an assortment of associated findings, including hyperactivity (86%), emotional lability (86%), joint deformities (71%), bone fractures (57%), abnormal sense of touch, vibration and position (50%), skin, hair and nails abnormalities (28%), and hypothermia episodes (28%). Two patients died at age 9 and 12 years from infection. In three cases, nerve conduction studies showed absent lower limbs sensory nerve action potentials. In one case, sensory nerve biopsy showed complete absence of unmyelinated fibers. Nine NTRK1 pathogenic variants were found, including three newly described mutations. This nationwide study confirms that NTRK1 gene-related CIPA is an extremely rare disorder and expands the genotypic spectrum of NTRK1 mutations.
先天性无痛无汗症(CIPA)是一种罕见的常染色体隐性遗传病,由编码神经营养酪氨酸激酶-1 受体的 NTRK1 基因突变引起。在这项多中心观察性回顾性研究中,我们调查了法国实验室通过测序 NTRK1 基因鉴定的 CIPA 患者,共发现了 7 名患者。患者来自法国(2 名)、苏里南(2 名)、马里(1 名)、哈萨克斯坦(1 名)和阿尔及利亚(1 名)。患者的平均年龄为 9.8 岁(4-20 岁),4 名患者为女性(57%),4 例患者婴儿期发育里程碑延迟(57%),4 例患者有近亲结婚史(57%)。诊断时的平均年龄为 4.8 个月(3-6 个月),所有患者均表现出无痛、无汗、智力障碍、自残、发热发作、体温感知受损和自主神经系统受损。患者还表现出一系列相关的发现,包括多动(86%)、情绪不稳定(86%)、关节畸形(71%)、骨折(57%)、异常触觉、振动和位置感(50%)、皮肤、毛发和指甲异常(28%)和体温过低发作(28%)。2 名患者分别在 9 岁和 12 岁时因感染死亡。在 3 例患者中,神经传导研究显示下肢感觉神经动作电位缺失。在 1 例患者中,感觉神经活检显示无髓纤维完全缺失。共发现 9 种 NTRK1 致病性变异,包括 3 种新描述的突变。这项全国性研究证实,NTRK1 基因相关的 CIPA 是一种极其罕见的疾病,并扩展了 NTRK1 基因突变的基因型谱。