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Rare association of Turner syndrome with neurofibromatosis type 1 and tuberous sclerosis complex

We report a rare association of Turner syndrome with both Neurofibromatosis type I and Tuberous Sclerosis. The patient had XOkaryotype with Turners stigmata and also had features of Neurofibromatosis 1 in the form of significant café-au-lait spots and Plexiform neurofibroma along with typical featur...

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Autores principales: Suttur, Malini S., Mysore, Savitha R., Krishnamurthy, Balasundaram, Nallur, Ramachandra B.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2910953/
https://www.ncbi.nlm.nih.gov/pubmed/20680156
http://dx.doi.org/10.4103/0971-6866.55220
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author Suttur, Malini S.
Mysore, Savitha R.
Krishnamurthy, Balasundaram
Nallur, Ramachandra B.
author_facet Suttur, Malini S.
Mysore, Savitha R.
Krishnamurthy, Balasundaram
Nallur, Ramachandra B.
author_sort Suttur, Malini S.
collection PubMed
description We report a rare association of Turner syndrome with both Neurofibromatosis type I and Tuberous Sclerosis. The patient had XOkaryotype with Turners stigmata and also had features of Neurofibromatosis 1 in the form of significant café-au-lait spots and Plexiform neurofibroma along with typical features of Tuberous Sclerosis complex. Pedigree analysis revealed that the elder brother of the proband in the family also suffered from Tuberous Sclerosis without the manifestation of Neurofibromatosis or any other genetic disorders. We hypothesize that these associations could be due to new independent mutations and also increased maternal and paternal age in a pre-disposition of Turner syndrome.
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spelling pubmed-29109532010-08-02 Rare association of Turner syndrome with neurofibromatosis type 1 and tuberous sclerosis complex Suttur, Malini S. Mysore, Savitha R. Krishnamurthy, Balasundaram Nallur, Ramachandra B. Indian J Hum Genet Case Report We report a rare association of Turner syndrome with both Neurofibromatosis type I and Tuberous Sclerosis. The patient had XOkaryotype with Turners stigmata and also had features of Neurofibromatosis 1 in the form of significant café-au-lait spots and Plexiform neurofibroma along with typical features of Tuberous Sclerosis complex. Pedigree analysis revealed that the elder brother of the proband in the family also suffered from Tuberous Sclerosis without the manifestation of Neurofibromatosis or any other genetic disorders. We hypothesize that these associations could be due to new independent mutations and also increased maternal and paternal age in a pre-disposition of Turner syndrome. Medknow Publications 2009 /pmc/articles/PMC2910953/ /pubmed/20680156 http://dx.doi.org/10.4103/0971-6866.55220 Text en © Indian Journal of Human Genetics http://creativecommons.org/licenses/by-nc-sa/2.0 This is an open-access article distributed under the terms of the Creative Commons Attribution license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Suttur, Malini S.
Mysore, Savitha R.
Krishnamurthy, Balasundaram
Nallur, Ramachandra B.
Rare association of Turner syndrome with neurofibromatosis type 1 and tuberous sclerosis complex
title Rare association of Turner syndrome with neurofibromatosis type 1 and tuberous sclerosis complex
title_full Rare association of Turner syndrome with neurofibromatosis type 1 and tuberous sclerosis complex
title_fullStr Rare association of Turner syndrome with neurofibromatosis type 1 and tuberous sclerosis complex
title_full_unstemmed Rare association of Turner syndrome with neurofibromatosis type 1 and tuberous sclerosis complex
title_short Rare association of Turner syndrome with neurofibromatosis type 1 and tuberous sclerosis complex
title_sort rare association of turner syndrome with neurofibromatosis type 1 and tuberous sclerosis complex
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2910953/
https://www.ncbi.nlm.nih.gov/pubmed/20680156
http://dx.doi.org/10.4103/0971-6866.55220
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