Cutaneous Findings in Ring Chromosome 7 Syndrome
Overview
Affiliations
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.
Multiple desmoplastic Spitz nevi with BRAF fusions in a patient with ring chromosome 7 syndrome.
Roy S, Bastian B, Maguiness S, Giubellino A, Vemula S, McCalmont T Pigment Cell Melanoma Res. 2021; 34(5):987-993.
PMID: 33522711 PMC: 9351601. DOI: 10.1111/pcmr.12963.
Ring chromosome 12 and severe oligospermia: a case report.
Martin J, Wold A, Taylor H Fertil Steril. 2007; 90(2):443.e13-5.
PMID: 17880954 PMC: 3107849. DOI: 10.1016/j.fertnstert.2007.07.1347.
Melanoma risk factors and atypical moles.
Williams M, Sagebiel R West J Med. 1994; 160(4):343-50.
PMID: 8023484 PMC: 1022426.
Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene?.
Pellegrino J, Schnur R, Kline R, Zackai E, Spinner N Hum Genet. 1995; 96(4):485-9.
PMID: 7557977 DOI: 10.1007/BF00191813.