Literature DB >> 8428052

Cutaneous findings in ring chromosome 7 syndrome.

S Vollenweider Roten1, I Masouyé, C D Delozier-Blanchet, J H Saurat.   

Abstract

All 9 cases of ring chromosome 7 syndrome already identified had skin lesions: 7 had vascular lesions, 5 showed large pigmented congenital nevi, 3 had café-au-lait spots and in 1 case there were achromic spots on the trunk. One girl developed malignant melanoma at the age of 17 years. It appears that in patients presenting with growth retardation and pigmented skin lesions, with or without mental retardation, a cytogenetic study is indicated to search for ring chromosome 7, which is probably more frequent than suggested by the literature.

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Year:  1993        PMID: 8428052     DOI: 10.1159/000247313

Source DB:  PubMed          Journal:  Dermatology        ISSN: 1018-8665            Impact factor:   5.366


  4 in total

1.  Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene?

Authors:  J E Pellegrino; R E Schnur; R Kline; E H Zackai; N B Spinner
Journal:  Hum Genet       Date:  1995-10       Impact factor: 4.132

Review 2.  Melanoma risk factors and atypical moles.

Authors:  M L Williams; R W Sagebiel
Journal:  West J Med       Date:  1994-04

3.  Ring chromosome 12 and severe oligospermia: a case report.

Authors:  J Ryan Martin; Anne Wold; Hugh S Taylor
Journal:  Fertil Steril       Date:  2007-09-19       Impact factor: 7.329

4.  Multiple desmoplastic Spitz nevi with BRAF fusions in a patient with ring chromosome 7 syndrome.

Authors:  Simon F Roy; Boris C Bastian; Sheilagh Maguiness; Alessio Giubellino; Swapna S Vemula; Timothy H McCalmont; Iwei Yeh
Journal:  Pigment Cell Melanoma Res       Date:  2021-03-17       Impact factor: 4.159

  4 in total

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