A rare case of patient with neurofibromatosis type 1 in a genotype-phenotype correlation revealing a submicroscopic deletion on the long arm of chromosome 17
Keyword(s):
We are reporting a case of neurofibromatosis type 1 in a genotype-phenotype correlation and chromosomal microarray test revealed a submicroscopic deletion on the long arm of chromosome 17, which is associated with a more severe phenotype. The presence of a more severe phenotype warrants precise monitoring of complications.
2015 ◽
Vol 23
(11)
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pp. 1460-1461
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2014 ◽
Vol 23
(4)
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pp. 244-247
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Keyword(s):
2020 ◽
Vol 29
(2)
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2016 ◽
Vol 5
(3)
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pp. 222
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