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Unique Roberts syndrome with bilateral congenital glaucoma: A case report
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作者 Amar Almulhim Basamat Almoallem +1 位作者 ehab alsirrhy Essam A Osman 《World Journal of Clinical Cases》 SCIE 2023年第19期4635-4639,共5页
BACKGROUND Congenital glaucoma associated with Roberts syndrome(RS)is an unusual and unique condition.No previous report describes this association.A multidisciplinary approach including molecular studies were conduct... BACKGROUND Congenital glaucoma associated with Roberts syndrome(RS)is an unusual and unique condition.No previous report describes this association.A multidisciplinary approach including molecular studies were conducted to reach the final diagnosis.CASE SUMMARY We present a rare case of a 1-wk-old male with RS associated with bilateral congenital glaucoma,left ectopic kidney,and left-hand rudimentary digits.A comprehensive approach was applied by which bilateral non-penetrating glaucoma surgery was performed with good control of intraocular pressure for more than 6 mo.Cytogenetic and molecular testing were conducted and revealed normal measurements.CONCLUSION This report described a case of a male baby with clinical features of RS but with a negative molecular analysis,presenting with left-hand rudimentary digits,bilateral congenital glaucoma,and left ectopic kidney.To the best of our knowledge,this is the first case reported with phocomelia,bilateral congenital glaucoma,and unilateral ectopic kidney. 展开更多
关键词 Roberts syndrome Roberts-SC phocomelia syndrome PHOCOMELIA Congenital glaucoma KARYOTYPE Whole exome sequencing Case report
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