Clinical genetics · 2000
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis.
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Palka G, Stuppia L, Guanciali Franchi P, Chiarelli F, Fischetto R, Borrelli P, Giannotti A, Fioretti G, Rinaldi M M, Mingarelli R, Rappold G A, Calabrese G
Аннотация
Twelve patients with different features of Turner syndrome, and with Xp and Yp rearrangements involving the pseudoautosomal region (PAR1) are described. In all patients, FISH analysis showed loss of one copy of the Short Stature Homeobox (SHOX)-containing gene. Ten patients had short stature and one disproportionate (mesomelic) normal stature, while the last one had normal stature. Skeletal abnormalities, including shortened ulna, were detected in nine subjects, and in six of them Madelung deformity was observed. These clinical data indicated a genotype phenotype correlation between haploinsufficiency of SHOX, and short stature and skeletal abnormalities.
Предметные рубрики MeSH
AdolescentAdultBody HeightBone Diseases, DevelopmentalBone and BonesChildChild, PreschoolChromosome AberrationsChromosome BandingFemaleGenotypeHomeodomain ProteinsHumansIn Situ Hybridization, FluorescenceInfantKaryotypingMalePhenotypePoint MutationRadiographyShort Stature Homeobox ProteinTurner SyndromeUlnaX ChromosomeY Chromosome