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Hennekam lymphangiectasia syndrome

Hennekam lymphangiectasia syndrome is a rare disorder comprising of intestinal and renal lymphangiectasia, dysmorphic facial appearance and mental retardation. The facial features include hypertelorism with a wide, flat nasal bridge, epicanthic folds, small mouth and small ears. We describe a case o...

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Detalles Bibliográficos
Autores principales: Lakshminarayana, G., Mathew, A., Rajesh, R., Kurien, G., Unni, V. N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3193672/
https://www.ncbi.nlm.nih.gov/pubmed/22022089
http://dx.doi.org/10.4103/0971-4065.78068
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author Lakshminarayana, G.
Mathew, A.
Rajesh, R.
Kurien, G.
Unni, V. N.
author_facet Lakshminarayana, G.
Mathew, A.
Rajesh, R.
Kurien, G.
Unni, V. N.
author_sort Lakshminarayana, G.
collection PubMed
description Hennekam lymphangiectasia syndrome is a rare disorder comprising of intestinal and renal lymphangiectasia, dysmorphic facial appearance and mental retardation. The facial features include hypertelorism with a wide, flat nasal bridge, epicanthic folds, small mouth and small ears. We describe a case of a multigravida with bad obstetric history and characteristic facial and dental anomalies and bilateral renal lymphangiectasia. To our knowledge this is the first case of Hennekam lymphangiectasia syndrome with anodontia to be reported from India.
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spelling pubmed-31936722011-10-21 Hennekam lymphangiectasia syndrome Lakshminarayana, G. Mathew, A. Rajesh, R. Kurien, G. Unni, V. N. Indian J Nephrol Case Report Hennekam lymphangiectasia syndrome is a rare disorder comprising of intestinal and renal lymphangiectasia, dysmorphic facial appearance and mental retardation. The facial features include hypertelorism with a wide, flat nasal bridge, epicanthic folds, small mouth and small ears. We describe a case of a multigravida with bad obstetric history and characteristic facial and dental anomalies and bilateral renal lymphangiectasia. To our knowledge this is the first case of Hennekam lymphangiectasia syndrome with anodontia to be reported from India. Medknow Publications 2011 /pmc/articles/PMC3193672/ /pubmed/22022089 http://dx.doi.org/10.4103/0971-4065.78068 Text en Copyright: © Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Lakshminarayana, G.
Mathew, A.
Rajesh, R.
Kurien, G.
Unni, V. N.
Hennekam lymphangiectasia syndrome
title Hennekam lymphangiectasia syndrome
title_full Hennekam lymphangiectasia syndrome
title_fullStr Hennekam lymphangiectasia syndrome
title_full_unstemmed Hennekam lymphangiectasia syndrome
title_short Hennekam lymphangiectasia syndrome
title_sort hennekam lymphangiectasia syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3193672/
https://www.ncbi.nlm.nih.gov/pubmed/22022089
http://dx.doi.org/10.4103/0971-4065.78068
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