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Genet Couns ; 13(1): 19-22, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-12017233

RESUMEN

Cleft lip (CL) and/or palate (CP) are uncommon anomalies in Turner syndrome (TS) series. We report two unrelated sporadic 46,X,i(Xq) patients exhibiting orofacial clefts and a peculiar facial appearance masking the clinical diagnosis. CL, and CP in case 1 and CP in case 2, though non-specific of TS, may not be fortuitous findings. The increased frequency of CP and bifid uvula in poly X syndromes, the dermatoglyphic similarities between iXq TS and X polysomies, and the occurrence of Klinefelter phenotype when extra Xq material is present in a male, are all indirect evidences suggesting that Xq material cannot be considered phenotipically inert and facial clefts found in our patients may be syndromal manifestation of trisomic Xq dosage.


Asunto(s)
Labio Leporino/genética , Fisura del Paladar/genética , Isocromosomas , Síndrome de Turner/genética , Niño , Preescolar , Femenino , Humanos , Úvula/anomalías
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