Mehta Viraj J, Ling Joseph J, Martinez Elizabeth G, Reddy Anvesh C, Donahue Sean P
Department of Ophthalmology (VJM, AR, SD), Vanderbilt Eye Institute, Nashville, Tennessee; Morehouse School of Medicine (JL), Atlanta, Georgia; and Department of Pathology, Microbiology, and Immunology (EGM), Vanderbilt University Medical Center, Nashville, Tennessee.
J Neuroophthalmol. 2016 Dec;36(4):414-416. doi: 10.1097/WNO.0000000000000405.
Autonomic dysfunction can be associated with pupillary abnormalities. We describe a rare association of tonic pupils, congenital central hypoventilation syndrome, and Hirschsprung disease in a newborn with a mutation in the PHOX2B gene, a key regulator of neural crest cells. Hirschsprung disease is characterized by the congenital absence of neural crest-derived intrinsic ganglion cells. Tonic pupils may result from an abnormality of the ciliary ganglion, another structure of neural crest origin. The close association of these conditions in this child suggests a common abnormality in neural crest migration and differentiation.
自主神经功能障碍可能与瞳孔异常有关。我们描述了一名新生儿中罕见的强直性瞳孔、先天性中枢性低通气综合征和先天性巨结肠病的关联,该新生儿的PHOX2B基因发生突变,PHOX2B基因是神经嵴细胞的关键调节因子。先天性巨结肠病的特征是先天性缺乏神经嵴衍生的内在神经节细胞。强直性瞳孔可能由睫状神经节异常引起,睫状神经节是另一种神经嵴起源的结构。该患儿中这些病症的密切关联提示神经嵴迁移和分化存在共同异常。