Dubowitz syndrome: common findings and peculiar urine odor

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 dise...

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Veröffentlicht in:Application of clinical genetics 2013-01, Vol.6 (default), p.87-90
Hauptverfasser: Chehade, Cynthia, Awwad, Johnny, Yazbeck, Nadine, Majdalani, Marianne, Wakim, Rima, Tfayli, Hala, Farra, Chantal
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Sprache:eng
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Zusammenfassung: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. We present here the case of a Lebanese girl with Dubowitz syndrome in whom an unpleasant urine odor was persistently reported since birth. 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.
ISSN:1178-704X
1178-704X
DOI:10.2147/TACG.S47777