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Terminal 2q deletion and partial trisomy chromosome 15q: a clinical and cytogenetic study

El-Bassyouni, H.T.; El-Gerzawy, A.M.S.; Mohamed, A.M.; Kamel, A.K.; Hussein, H.A.; Thomas, M.M.; El-Ruby, M.

Genetic Counseling 25(2): 151-158

2014

ISSN/ISBN: 1015-8146
PMID: 25059013
Document Number: 678670
We report on a 5 years old female patient with a karyotype 46, XX, add (2), t(2;15) (q37;q22) associated with dysmorphic facial features, digital deformities, heart defect (mild mitral regurge) and severe mental retardation. This is the third reported case worldwide on the terminal 2q deletion and trisomy of chromosome 15q syndrome. The findings in this case and our literature review, delineates the pattern of malformations secondary to trisomy of 15q and deletion of 2q.

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