Artigo Revisado por pares

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

1992; Elsevier BV; Volume: 339; Issue: 8802 Linguagem: Inglês

10.1016/0140-6736(92)90734-k

ISSN

1474-547X

Autores

Peter Scambler, David A. Kelly, Elizabeth Lindsay, R. Williamson, Rosalie Goldberg, Robert J. Shprintzen, David I. Wilson, Judith A. Goodship, I E Cross, John Burn,

Tópico(s)

Tissue Engineering and Regenerative Medicine

Resumo

The large clinical overlap between DiGeorge syndrome and velo-cardio-facial syndrome suggests an aetiological connection. DiGeorge syndrome is associated with microdeletions of chromosome 22q11 and is therefore likely to be caused by reduced dosage of genes within this region. We present preliminary data that velocardiofacial syndrome patients have similar chromosome deletions, a finding consistent with the hypothesis that these disorders represent part of a spectrum of abnormalities seen with monosomy for 22q11.

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