Khan Arif O, Al-Mesfer Saleh
Division of Pediatric Ophthalmology, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Division of Pediatric Ophthalmology, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.
J AAPOS. 2015 Oct;19(5):463-5. doi: 10.1016/j.jaapos.2015.04.011.
Congenital cranial dysinnervation disorders are phenotypes of incomitant strabismus and/or ptosis. Recessive mutations in COL25A1 are a recently reported cause, but the associated ophthalmic phenotypes have not been detailed. We highlight phenotypes of the 4 affected children from the 2 reported families: isolated congenital ptosis (one unilateral, one bilateral) and Duane syndrome (one unilateral, one bilateral) with synergistic divergence. Further study is needed to understand how frequently recessive COL25A1 mutations underlie these specific ocular phenotypes.
先天性颅神经支配障碍是一种伴有斜视和/或上睑下垂的表型。COL25A1基因的隐性突变是最近报道的病因,但相关的眼科表型尚未详细描述。我们重点介绍了2个已报道家族中4名患病儿童的表型:孤立性先天性上睑下垂(1例单侧,1例双侧)和伴有协同性散开的杜安综合征(1例单侧,1例双侧)。需要进一步研究以了解隐性COL25A1突变导致这些特定眼部表型的频率。