Excessively redundant umbilical skin as a potential early clinical feature of Morquio syndrome and FKBP14-related Ehlers-Danlos syndrome

被引:16
作者
Aldeeri, A. A. [1 ]
Alazami, A. M. [1 ]
Hijazi, H. [1 ]
Alzahrani, F. [1 ]
Alkuraya, F. S. [1 ,2 ]
机构
[1] King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia
[2] Alfaisal Univ, Coll Med, Dept Anat & Cell Biol, Riyadh, Saudi Arabia
关键词
dysmorphology; hypermobility; mucopolysaccharidosis; umbilicus; IVA MORQUIO; RIEGER-SYNDROME; BELLY BUTTON; LENGTH;
D O I
10.1111/cge.12414
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Several umbilical abnormalities have been linked to and utilized to aid in the clinical diagnosis of certain syndromes. For instance, umbilical skin redundancy has long been recognized as a core feature of Rieger syndrome although its association with other disorders is unknown. In this article, we report for the first time the occurrence of this distinct clinical sign in association with two other syndromes: Morquio syndrome and FKBP14-related Ehlers-Danlos syndrome (EDS). Our observation is clinically significant because patients with Morquio syndrome are often diagnosed only after they develop typical skeletal manifestations, which reduces the efficacy of available enzyme replacement therapy, so the umbilical sign we report here can facilitate a much earlier diagnosis. In addition, the extreme rarity of FKBP14-related Ehlers-Danlos syndrome (EDS) can greatly delay the diagnosis of this condition unless it is recognized in the differential diagnosis of redundant umbilical skin as we argue in this report.
引用
收藏
页码:469 / 472
页数:4
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