Dubowitz syndrome: common findings and peculiar urine odor

被引:2
作者
Chehade, Cynthia [1 ]
Awwad, Johnny [2 ]
Yazbeck, Nadine [1 ]
Majdalani, Marianne [1 ]
Wakim, Rima [1 ]
Tfayli, Hala [1 ]
Farra, Chantal [1 ,3 ]
机构
[1] Amer Univ Beirut, Med Ctr, Dept Pediat & Adolescent Med, POB 11-0236,Riad El Solh, Beirut 11072020, Lebanon
[2] Amer Univ Beirut, Med Ctr, Dept Obstet & Ginecol, Beirut, Lebanon
[3] Amer Univ Beirut, Med Ctr, Dept Pathol & Lab Med, Beirut, Lebanon
关键词
Dubowitz syndrome; autosomal recessive; developmental delay; odorous urine;
D O I
10.2147/TACG.S47777
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Background: Dubowitz syndrome is a rare, autosomal recessive disorder characterized by intrauterine and postnatal growth retardation, severe microcephaly, psychomotor retardation, hyperactivity, eczema, and characteristic dysmorphic facial features. Although many cases have been reported, the cause of this disease is still unknown. Case: We present here the case of a Lebanese girl with Dubowitz syndrome in whom an unpleasant urine odor was persistently reported since birth. Conclusion: Although Dubowitz syndrome has been largely described in the medical literature, this is the first time that a peculiar urine odor was reported. This case report adds a new and unusual feature to the numerous findings related to this rare polymorphous syndrome.
引用
收藏
页码:87 / 90
页数:4
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