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Indian J Hum Genet ; 2009 May; 15(2): 75-77
Artículo en Inglés | IMSEAR | ID: sea-138875

RESUMEN

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.


Asunto(s)
Femenino , Humanos , Neurofibromatosis 1/diagnóstico , Neurofibromatosis 1/epidemiología , Neurofibromatosis 1/etiología , Neurofibromatosis 1/genética , Hermanos , Esclerosis Tuberosa/diagnóstico , Esclerosis Tuberosa/epidemiología , Esclerosis Tuberosa/etiología , Esclerosis Tuberosa/genética , Síndrome de Turner/diagnóstico , Síndrome de Turner/epidemiología , Síndrome de Turner/etiología , Síndrome de Turner/genética , Adulto Joven
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