Unique Combination of 22q11 and 14qter Microdeletion Syndromes Detected Using Oligonucleotide Array-CGH

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Authors

HLADÍLKOVÁ Eva VRANOVÁ Vladimíra ŠOUKALOVÁ Jana SLÁMOVÁ Iva VILÉMOVÁ Marcela GAILLYOVÁ Renata KUGLÍK Petr

Year of publication 2012
Type Article in Periodical
Magazine / Source Molecular Syndromology
MU Faculty or unit

Faculty of Science

Citation
Web http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowAbstract&ArtikelNr=335334&Ausgabe=256796&ProduktNr=247640
Doi http://dx.doi.org/10.1159/000335334
Field Genetics and molecular biology
Keywords 14qter microdeletion syndrome; Array-CGH; Deletion 14q; Deletion 22q1; DiGeorge syndrome; Velocardiofacial syndrome
Description We report an infant with a unique combination of 22q11 deletion syndrome and 14q terminal deletion syndrome. The proband had clinical symptoms compatible with diagnosis of 22q11 deletion syndrome: microcephaly, micrognathia, high-arched palate, hypertelorism, short palpebral fissures, square nasal root, prominent tubular nose, hypoplastic nasal alae, bulbous nasal tip, dysplastic low-set ears, short philtrum, and heart defect, but no cell-mediated immunodeficiency typical for the syndrome. G-banding and fluorescence in situ hybridization analyses revealed a karyotype 45,XY,der(14)t(14;22)(q32.3;q11.2),-22.ish del(14)(q32.33)(D14S1420-),del(22)(q11.2q11.2)(N25-). Subsequent analyses disclosed a translocation between chromosomes 14 and 22 in the proband’s mother with a deleted 14q telomere. Using comparative genome hybridization on oligonucleotide-based microarray (array-CGH), the deletion at 22q11.21 in the size of 4.25 Mb was revealed in the proband as well as the deletion of the telomeric area at 14q32.33qter (3.24 Mb) in the proband and his mother. However, both the proband and his mother showed mild symptoms (microcephaly, thin lips, carp-shaped mouth) typical for patients with the described terminal 14q deletion syndrome.
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