Menges-Wenzel E M, Kurlemann G, Pawlowitzki J H
Neuropädiatrischer Bereich, Universitäts-Kinderklinik, Universität Münster.
Monatsschr Kinderheilkd. 1993 Dec;141(12):922-4.
Two children with progressive facial atrophia are described. In both asymmetria of the face was the reason for neuropediatric examination. Discrete neurological symptoms of this neurocutaneous syndrome were found. In patient 1 atrophia of one side of the face had developed shortly after surgical treatment of a mandibular exostose on the other side of the face. In patient 2 first signs of hemifacial atrophia were found in the newborn. Both children showed only discrete neurological symptoms. Etiology of this rare disease is still unknown, causal treatment is not possible.
本文描述了两名患有进行性面部萎缩症的儿童。面部不对称是这两名儿童接受神经儿科检查的原因。发现了这种神经皮肤综合征的一些轻微神经症状。在患者1中，一侧面部萎缩是在对面下颌外生骨手术治疗后不久出现的。在患者2中，在新生儿期发现了半侧面部萎缩的最初迹象。两名儿童均仅表现出轻微的神经症状。这种罕见疾病的病因仍然不明，无法进行病因治疗。
