APHP, Centre de référence des maladies neuromusculaires, Institut de Myologie, Sorbonne Université, APHP, Hôpital Pitié-Salpêtrière; Paris, France.
UF de neurogénétique héreditaire (UF 34427), Centre de Biologie et Pathologie Est - Service de Biochimie Biologie Moléculaire Grande Est; Hospices Civils, Lyon, France.
Neuromuscul Disord. 2020 Jul;30(7):576-582. doi: 10.1016/j.nmd.2020.05.003. Epub 2020 May 16.
We report seven Charcot-Marie-Tooth 4B1 (CMT4B1) patients from four families with distinctive features, presenting with severe distal weakness and cranial nerve involvement. Patient from family 1 presented with congenital varus foot deformity, progressive distal and proximal weakness leading to loss of ambulation at 14 years, bilateral facial palsy and prominent bulbar involvement. In three siblings from family 2, still ambulant in the second decade, neuropathy was associated with marked sweating and Arnold-Chiari syndrome. Patient from family 3, wheelchair-bound by 17 years, suffered from recurrent intestinal occlusion due to a mesenteric malformation. Patients from family 4, wheelchair-bound from age 6 years, were first diagnosed with type 1 Usher syndrome with congenital deafness and retinitis pigmentosa. CMT4B1 diagnosis was based upon suggestive clinical features and confirmed by the presence of recessive mutations in the MTMR2 gene. Our results expand the genetic and phenotypic spectrum of CMT4B1, which may include autonomic system involvement.
我们报告了来自四个家庭的 7 名腓骨肌萎缩症 4B1(CMT4B1)患者,他们具有独特的特征,表现为严重的远端肌无力和颅神经受累。1 号家庭的患者表现为先天性足内翻畸形,进行性远端和近端肌无力,导致 14 岁时丧失行走能力,双侧面瘫和明显的球部受累。2 号家庭的 3 名兄弟姐妹,在 20 多岁时仍能行走,神经病变伴有明显的出汗和 Arnold-Chiari 综合征。3 号家庭的患者 17 岁时已坐上轮椅,因肠系膜畸形而反复发生肠梗阻。4 号家庭的患者自 6 岁起已坐上轮椅,最初被诊断为 1 型 Usher 综合征,伴有先天性耳聋和视网膜色素变性。CMT4B1 的诊断基于提示性的临床特征,并通过 MTMR2 基因的隐性突变得到证实。我们的结果扩展了 CMT4B1 的遗传和表型谱,其中可能包括自主神经系统受累。