Brown syndrome associated with velocardiofacial syndrome

Occurrences of Brown syndrome are rare, hence the difficulty in establishing the exact etiology. We report a patient with Brown syndrome associated with velocardiofacial syndrome (deletion of chromosome 22q11), which may implicate a candidate chromosomal region for some cases of this syndrome.

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Bibliographische Detailangaben
Veröffentlicht in:	Journal of AAPOS 2004-06, Vol.8 (3), p.290-292
Hauptverfasser:	Chang, Susie, Crowe, Carol A, Traboulsi, Elias I
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities, Multiple Child, Preschool Chromosome Deletion Chromosomes, Human, Pair 22 Craniofacial Abnormalities - complications Craniofacial Abnormalities - genetics Female Heart Defects, Congenital - complications Heart Defects, Congenital - genetics Humans In Situ Hybridization, Fluorescence Karyotyping Ocular Motility Disorders - complications Ocular Motility Disorders - genetics
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Beschreibung
Zusammenfassung:	Occurrences of Brown syndrome are rare, hence the difficulty in establishing the exact etiology. We report a patient with Brown syndrome associated with velocardiofacial syndrome (deletion of chromosome 22q11), which may implicate a candidate chromosomal region for some cases of this syndrome.
ISSN:	1091-8531 1528-3933
DOI:	10.1016/j.jaapos.2004.01.012