A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features.
- Molin, A.M.
- Andrieux, J.
- Koolen, D.A.
- Malan, V.
- Carella, M.
- Colleaux, L.
- Cormier-Daire, V.
- David, A.
- Leeuw, N. de
- Delobel, B.
- Duban-Bedu, B.
- Fischetto, R.
- Flinter, F.
- Kjaergaard, S.
- Kok, F.
- Krepischi, A.C.
- Caignec, C. Le
- Ogilvie, C.M.
- Maia, S.
- Mathieu-Dramard, M.
- Munnich, A.
- Palumbo, O.
- Papadia, F.
- Pfundt, R.
- Reardon, W.
- Receveur, A.
- Rio, M. del
- Ronsbro Darling, L.
- Rosenberg, C.
- Sa, J.
- Vallee, L.
- Vincent-Delorme, C.
- Zelante, L.
- Bondeson, M.L.
- Anneren, G.
DOIAbstract
Item does not contain fulltextBACKGROUND: Congenital deletions affecting 3q11q23 have rarely been reported and only five cases have been molecularly characterised. Genotype-phenotype correlation has been hampered by the variable sizes and breakpoints of the deletions. In this study, 14 novel patients with deletions in 3q11q23 were investigated and compared with 13 previously reported patients. METHODS: Clinical data were collected from 14 novel patients that had been investigated by high resolution microarray techniques. Molecular investigation and updated clinical information of one cytogenetically previously reported patient were also included. RESULTS: The molecular investigation identified deletions in the region 3q12.3q21.3 with differ...
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