Thomas Quentin, Morgant Marie-Catherine, Nambot Sophie, Thauvin-Robinet Christel, Giroud Maurice
Inserm UMR1231 Team GAD, University of Burgundy and Franche-Comté, F-21000, Dijon, France.
Department of Neurology, Dijon Bourgogne University Hospital, F-21000, Dijon, France.
Neurol Sci. 2023 Apr;44(4):1207-1210. doi: 10.1007/s10072-022-06534-6. Epub 2022 Dec 2.
Facial asymmetry when crying at birth (then called asymmetric crying facies or ACF) or when smiling or speaking loudly in adulthood is the consequence of the agenesis or hypoplasia of the muscle of one of the labial commissures. This developmental disorder of complex mechanism is well known by pediatricians to be a warning sign for underlying developmental disorders of variable severity.
An 80-year-old man with medical history of renal agenesis was hospitalized for a transient motor deficit of the right face and arm revealing a lacunar stroke. Clinical examination showed an isolated left facial asymmetry upon smiling or talking out loud which had been known since childhood and was not related to the stroke, leading to the diagnosis of ACF. Cardiac ultrasound revealed a patent foramen. Chromosomal investigations could not be performed.
ACF is a rare disorder that may conceal associated congenital disorders such as heart, skeletal, or renal malformations. Its causing mechanisms are to this day still poorly understood but may include a genetic component as shown by familial cases and the identification of 22q11.2 deletions or trisomy 18 in some patients. Knowledge of this disorder seems highly relevant for adult neurologists, first because of the differential diagnosis with facial palsy, but mostly because it will allow them to screen patients for other congenital disorders such as heart malformations. Conversely, cardiologists and cardiac surgeon may search for an ACF when faced with a patient with a congruent heart defect.
出生时哭泣时面部不对称(当时称为不对称哭泣面容或ACF)或成年后微笑或大声说话时面部不对称是一侧唇联合肌发育不全或发育不良的结果。儿科医生熟知这种机制复杂的发育障碍是潜在不同严重程度发育障碍的警示信号。
一名有肾发育不全病史的80岁男性因右侧面部和手臂短暂运动功能缺损入院,诊断为腔隙性中风。临床检查发现,患者自童年起就存在孤立的左侧面部不对称,在微笑或大声说话时出现,与中风无关,诊断为ACF。心脏超声显示卵圆孔未闭。无法进行染色体检查。
ACF是一种罕见疾病,可能掩盖相关先天性疾病,如心脏、骨骼或肾脏畸形。其致病机制至今仍知之甚少,但可能包括遗传因素,如家族性病例所示,以及一些患者中发现的22q11.2缺失或18三体。对于成年神经科医生来说,了解这种疾病似乎非常重要,首先是因为要与面瘫进行鉴别诊断,但主要是因为这将使他们能够对患者进行其他先天性疾病筛查,如心脏畸形。相反,心脏病专家和心脏外科医生在面对患有先天性心脏缺陷的患者时,可能会检查是否存在ACF。