Literature DB >> 6810767

Café-au-lait spots in schoolchildren.

R G Burwell, N J James, D I Johnston.   

Abstract

This paper reports a study of café-au-lait spots of a minimum diameter of 1 cm in 732 white schoolchildren. Three groups were identified, according to the number of café-au-lait spots on each child: (1) those with none (74%), (2) those with fewer than 5 (25%), and (3) those with at least 5 (5 children, 2 considered to be normal, and 3 siblings each presumed to have neurofibromatosis, one having died from leukaemia). Excluding the last group, the number of café-au-lait spots in the sample was not significantly related to age or sex. Some support is given for using the number of café-au-lait spots as an empirical threshold to diagnose neurofibromatosis.

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Year:  1982        PMID: 6810767      PMCID: PMC1627749          DOI: 10.1136/adc.57.8.631

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  5 in total

1.  Birthmarks with serious medical significance: nevocullular nevi, sebaceous nevi, and multiple café au lait spots.

Authors:  J Alper; L B Holmes; M C Mihm
Journal:  J Pediatr       Date:  1979-11       Impact factor: 4.406

2.  Diagnostic value of the café-au-lait spot in children.

Authors:  D Whitehouse
Journal:  Arch Dis Child       Date:  1966-06       Impact factor: 3.791

Review 3.  Perthes' disease: a concept of pathogenesis.

Authors:  M H Harrison; R G Burwell
Journal:  Clin Orthop Relat Res       Date:  1981-05       Impact factor: 4.176

4.  No maternal effect in childhood leukaemia with neurofibromatosis.

Authors:  J I Bader; R W Miller
Journal:  Lancet       Date:  1979-03-03       Impact factor: 79.321

5.  Pathophysiology of neurofibromatosis. IV. Dermatologic insights into heterogeneity and pathogenesis.

Authors:  V M Riccardi
Journal:  J Am Acad Dermatol       Date:  1980-08       Impact factor: 11.527

  5 in total
  5 in total

Review 1.  A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counselling.

Authors:  S M Huson; D A Compston; P S Harper
Journal:  J Med Genet       Date:  1989-11       Impact factor: 6.318

2.  Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome.

Authors:  Michel De Vos; Bruce E Hayward; Susan Picton; Eamonn Sheridan; David T Bonthron
Journal:  Am J Hum Genet       Date:  2004-04-07       Impact factor: 11.025

Review 3.  Challenges in the diagnosis of neurofibromatosis type 1 (NF1) in young children facilitated by means of revised diagnostic criteria including genetic testing for pathogenic NF1 gene variants.

Authors:  Hildegard Kehrer-Sawatzki; David N Cooper
Journal:  Hum Genet       Date:  2021-12-20       Impact factor: 4.132

4.  Diagnostic and pathogenetic role of café-au-lait macules in nevoid basal cell carcinoma syndrome.

Authors:  Giovanni Ponti; Aldo Tomasi; Lorenza Pastorino; Cristel Ruini; Carmelo Guarneri; Victor Desmond Mandel; Stefania Seidenari; Giovanni Pellacani
Journal:  Hered Cancer Clin Pract       Date:  2012-10-29       Impact factor: 2.857

5.  Prevalence of Café-au-Lait Spots in children with solid tumors.

Authors:  Anna Claudia Evangelista Dos Santos; Benjamin Heck; Beatriz De Camargo; Fernando Regla Vargas
Journal:  Genet Mol Biol       Date:  2016-05-24       Impact factor: 1.771

  5 in total

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