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Dubowitz syndrome: common findings and peculiar urine odor

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...

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Autores principales: Chehade, Cynthia, Awwad, Johnny, Yazbeck, Nadine, Majdalani, Marianne, Wakim, Rima, Tfayli, Hala, Farra, Chantal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3805180/
https://www.ncbi.nlm.nih.gov/pubmed/24159261
http://dx.doi.org/10.2147/TACG.S47777
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author Chehade, Cynthia
Awwad, Johnny
Yazbeck, Nadine
Majdalani, Marianne
Wakim, Rima
Tfayli, Hala
Farra, Chantal
author_facet Chehade, Cynthia
Awwad, Johnny
Yazbeck, Nadine
Majdalani, Marianne
Wakim, Rima
Tfayli, Hala
Farra, Chantal
author_sort Chehade, Cynthia
collection PubMed
description 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.
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spelling pubmed-38051802013-10-24 Dubowitz syndrome: common findings and peculiar urine odor Chehade, Cynthia Awwad, Johnny Yazbeck, Nadine Majdalani, Marianne Wakim, Rima Tfayli, Hala Farra, Chantal Appl Clin Genet Case Report 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. Dove Medical Press 2013-10-08 /pmc/articles/PMC3805180/ /pubmed/24159261 http://dx.doi.org/10.2147/TACG.S47777 Text en © 2013 Chehade et al. This work is published by Dove Medical Press Ltd, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Ltd, provided the work is properly attributed.
spellingShingle Case Report
Chehade, Cynthia
Awwad, Johnny
Yazbeck, Nadine
Majdalani, Marianne
Wakim, Rima
Tfayli, Hala
Farra, Chantal
Dubowitz syndrome: common findings and peculiar urine odor
title Dubowitz syndrome: common findings and peculiar urine odor
title_full Dubowitz syndrome: common findings and peculiar urine odor
title_fullStr Dubowitz syndrome: common findings and peculiar urine odor
title_full_unstemmed Dubowitz syndrome: common findings and peculiar urine odor
title_short Dubowitz syndrome: common findings and peculiar urine odor
title_sort dubowitz syndrome: common findings and peculiar urine odor
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3805180/
https://www.ncbi.nlm.nih.gov/pubmed/24159261
http://dx.doi.org/10.2147/TACG.S47777
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