Literature DB >> 18712027

Segmental neurofibromatosis associated with renal angiomyolipomas.

Kim-Tan Nguyen1, Melvin Chiu.   

Abstract

Segmental neurofibromatosis (SN) is a rare disorder characterized by neurofibromas or neurofibromas with café-au-lait spots limited to one region of the body without crossing the midline. Renal angiomyolipomas (AMLs) are rare benign neoplasms usually found in association with tuberous sclerosis (TS). Similar to neurofibromatosis (NF), TS has a high spontaneous mutation rate and a family history often is absent. Although both are autosomal dominant diseases with neural involvement, there are few reports in the literature demonstrating a link between the 2 disorders. We report a case of SN associated with renal AMLs. To our knowledge, there has been only 1 prior report of renal AML associated with NF type 1 (NF1), and there have been no prior reports of SN associated with AML.

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Mesh:

Year:  2008        PMID: 18712027

Source DB:  PubMed          Journal:  Cutis        ISSN: 0011-4162


  2 in total

1.  Renal manifestations in children with neurofibromatosis type 1.

Authors:  Binnaz Celik; Ozlem Yuksel Aksoy; Funda Bastug; Hatice Gamze Poyrazoglu
Journal:  Eur J Pediatr       Date:  2021-06-06       Impact factor: 3.183

2.  NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders.

Authors:  Valentina La Cognata; Giovanna Morello; Giulia Gentile; Francesca Cavalcanti; Rita Cittadella; Francesca Luisa Conforti; Elvira Valeria De Marco; Angela Magariello; Maria Muglia; Alessandra Patitucci; Patrizia Spadafora; Velia D'Agata; Martino Ruggieri; Sebastiano Cavallaro
Journal:  Curr Genomics       Date:  2018-09       Impact factor: 2.236

  2 in total

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