Literature DB >> 8456833

Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage.

J Charrow1, R Listernick, K Ward.   

Abstract

Multiple café-au-lait spots have been observed in successive generations of several families without any other manifestations of neurofibromatosis (NF) or any other systemic disorder. The café-au-lait spots in these families segregate as an autosomal dominant trait. The relationship (if any) between the gene for this trait and the NF-1 gene has previously been unknown. We describe a family with five individuals spanning four generations with dominantly inherited café-au-lait spots, without any other stigmata of NF-1. Linkage analysis with probes proximal, distal, and within the NF-1 gene indicate that the trait in this family is not linked to NF-1. We propose that this condition be called Familial Café-Au-Lait Spots (FCAL) to distinguish it from the neurofibromatosis syndromes.

Entities:  

Mesh:

Year:  1993        PMID: 8456833     DOI: 10.1002/ajmg.1320450518

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  7 in total

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2.  Hereditary spinal neurofibromatosis: a rare form of NF1?

Authors:  M Poyhonen; E L Leisti; S Kytölä; J Leisti
Journal:  J Med Genet       Date:  1997-03       Impact factor: 6.318

3.  Two pathogenic NF1 gene mutations identified in DNA from a child with mild phenotype.

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Journal:  Childs Nerv Syst       Date:  2011-12-09       Impact factor: 1.475

4.  SPRED 1 mutations in a neurofibromatosis clinic.

Authors:  Talia M Muram-Zborovski; David A Stevenson; David H Viskochil; David C Dries; Andrew R Wilson
Journal:  J Child Neurol       Date:  2010-02-22       Impact factor: 1.987

5.  An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation.

Authors:  M Upadhyaya; S M Huson; M Davies; N Thomas; N Chuzhanova; S Giovannini; D G Evans; E Howard; B Kerr; S Griffiths; C Consoli; L Side; D Adams; M Pierpont; R Hachen; A Barnicoat; H Li; P Wallace; J P Van Biervliet; D Stevenson; D Viskochil; D Baralle; E Haan; V Riccardi; P Turnpenny; C Lazaro; L Messiaen
Journal:  Am J Hum Genet       Date:  2006-12-08       Impact factor: 11.025

6.  Familial café au lait spots: a variant of neurofibromatosis type 1.

Authors:  D Abeliovich; Z Gelman-Kohan; S Silverstein; I Lerer; J Chemke; S Merin; J Zlotogora
Journal:  J Med Genet       Date:  1995-12       Impact factor: 6.318

Review 7.  Neurofibromatosis type 1.

Authors:  Kevin P Boyd; Bruce R Korf; Amy Theos
Journal:  J Am Acad Dermatol       Date:  2009-07       Impact factor: 11.527

  7 in total

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