Literature DB >> 9263313

Neurofibromatosis and reticulate acropigmentation of Dohi: a case report.

H H Tan1, Y K Tay.   

Abstract

A 13-year-old boy had progressive pigmentary changes affecting his limbs which began when he was 9 months of age. He also had a history of café au lait macules on his trunk since birth which were becoming more numerous. The diagnosis of reticulate acropigmentation of Dohi (dyschromatosis symmetrica hereditaria) and neurofibromatosis type 1 (NF-1) was made on the basis of the clinical features. To our knowledge, this is the first report of these two conditions occurring in the same patient.

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Year:  1997        PMID: 9263313     DOI: 10.1111/j.1525-1470.1997.tb00962.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  2 in total

1.  A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2.

Authors:  Qing-he Xing; Ming-tai Wang; Xiang-dong Chen; Guo-yin Feng; Hong-yun Ji; Jian-dong Yang; Jian-jun Gao; Wei Qin; Xue-qing Qian; Sheng-nan Wu; Lin He
Journal:  Am J Hum Genet       Date:  2003-06-12       Impact factor: 11.025

2.  Dyschromatosis symmetrica hereditaria with cutaneous lupus erythematosus and hyperthyroidism.

Authors:  Fahad Al-Saif; Ahmed Alhumidi; Rama Ayed Alhallaf
Journal:  Int Med Case Rep J       Date:  2017-05-02
  2 in total

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