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Blaschkolinear malformation syndrome in complex trisomy-7 mosaicism

✍ Scribed by Magenis, Ellen; Webb, Mary Jane; Spears, Becky; Opitz, John M.


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
73 KB
Volume
87
Category
Article
ISSN
0148-7299
DOI
10.1002/(sici)1096-8628(19991222)87:5<375::aid-ajmg2>3.0.co;2-w

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✦ Synopsis


Results of repeated peripheral blood chromosome studies were normal in a boy with intrauterine growth retardation, short stature, moderate mental retardation, and multiple minor anomalies. At age 9 years it was recognized that the swirls of pigmentation/ depigmentation on his trunk, linear streaks on his limbs, and body asymmetry were suggestive of chromosomal mosaicism. Four skin biopsies were obtained under anesthesia during a dental procedure. All showed mosaicism for a normal cell line, a line with an extra chromosome 7, and a cell line with an extra small ring. In one biopsy, there was a fourth cell line with an extra chromosome 7 and the ring. Fluorescence in situ hybridization (FISH) with a chromosome 7 paint confirmed trisomy 7 and the chromosome 7 derivation of the ring. This young man's intra-uterine and postnatal growth retardation is an aneuploidy effect, whereas his asymmetry reflects a mosaicism effect that should have aroused suspicion of tissuelimited mosaicism before the development of obvious Blaschkolinear skin pigmentary dysplasia. Am. J. Med. Genet. 87:375-383, 1999.


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