A SIBSHIP WITH UNUSUAL ANOMALIES OF THE EYE AND SKELETON (MICHELS SYNDROME)

被引:14
作者
DELAPAZ, MA
LEWIS, RA
PATRINELY, JR
MERIN, L
GREENBERG, F
机构
[1] MASSACHUSETTS EYE & EAR HOSP, DEPT OPHTHALMOL, BOSTON, MA 02114 USA
[2] BAYLOR COLL MED, INST MOLEC GENET, DEPT OPHTHALMOL, HOUSTON, TX 77030 USA
[3] BAYLOR COLL MED, INST MOLEC GENET, DEPT PEDIAT, HOUSTON, TX 77030 USA
[4] BAYLOR COLL MED, DIV PLAST SURG, HOUSTON, TX 77030 USA
关键词
D O I
10.1016/S0002-9394(14)76861-8
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Four siblings of nonconsanguineous parents had congenital anomalies of the anterior segment of the eyes, eyelids, and skeletal systems. Anomalies of the anterior segment included opacities of the corneal stroma, conjunctival telangiectasia, and iridocorneal adhesions. Eyelid abnormalities included blepharoptosis, blepharophimosis, and telecanthus. One sibling with extensive anterior segment anomalies developed glaucoma. All subjects had impaired vertical gaze. Oromandibular anomalies varied from cleft lip and palate to malocclusion with overbite. Additional features included subnormal intelligence, short stature, hearing loss, and clinodactyly. This spectrum of anomalies appeared to have been transmitted as an autosomal recessive syndrome.
引用
收藏
页码:572 / 580
页数:9
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