Literature DB >> 15637706

Simultaneous occurrence of neurofibromatosis type 1 and tuberous sclerosis in a young girl.

Patricia G Wheeler1, Ab Sadeghi-Nejad.   

Abstract

Neurofibromatosis type 1 and tuberous sclerosis are the two most common neurocutaneous disorders in humans. Both are transmitted as autosomal dominant conditions with a high rate of new mutations and similar clinical features. However, the two disorders have distinct and well-delineated genetic, biochemical, and physical findings. Simultaneous occurrence of these two conditions is rare. We report on a young girl who inherited both disorders, review similar cases reported in the world literature, and discuss possible implications of the presence of NF1 and TSC in the same individual. (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15637706     DOI: 10.1002/ajmg.a.30530

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  3 in total

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

Authors:  Malini S Suttur; Savitha R Mysore; Balasundaram Krishnamurthy; Ramachandra B Nallur
Journal:  Indian J Hum Genet       Date:  2009-05

2.  A Potential Role for Felbamate in TSC- and NF1-Related Epilepsy: A Case Report and Review of the Literature.

Authors:  Natanya M Mishal; Dimitrios Arkilo; Ju Tang; John R Crawford; Sonya G Wang
Journal:  Case Rep Neurol Med       Date:  2015-10-22

3.  Co-occurrence of neurofibromatosis type 1 and optic nerve gliomas with autosomal dominant polycystic kidney disease type 2.

Authors:  Ramón Peces; Rocío Mena; Yolanda Martín; Concepción Hernández; Carlos Peces; Dolores Tellería; Emilio Cuesta; Rafael Selgas; Pablo Lapunzina; Julián Nevado
Journal:  Mol Genet Genomic Med       Date:  2020-06-13       Impact factor: 2.183

  3 in total

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