PT  - JOURNAL ARTICLE
AU  - B Lecumberri
AU  - E Fernández-Rebollo
AU  - L Sentchordi
AU  - P Saavedra
AU  - A Bernal-Chico
AU  - L F Pallardo
AU  - J M Jiménez Bustos
AU  - L Castaño
AU  - M de Santiago
AU  - O Hiort
AU  - G Pérez de Nanclares
AU  - M Bastepe
TI  - Coexistence of two different pseudohypoparathyroidism subtypes (Ia and Ib) in the same kindred with independent Gsα coding mutations and <em>GNAS</em> imprinting defects
AID  - 10.1136/jmg.2009.071001
DP  - 2010 Apr 01
TA  - Journal of Medical Genetics
PG  - 276--280
VI  - 47
IP  - 4
4099  - http://jmg.bmj.com/content/47/4/276.short
4100  - http://jmg.bmj.com/content/47/4/276.full
SO  - J Med Genet2010 Apr 01; 47
AB  - Background Pseudohypoparathyroidism (PHP) defines a rare group of disorders whose common feature is resistance to the parathyroid hormone. Patients with PHP-Ia display additional hormone resistance, Albright hereditary osteodystrophy (AHO) and reduced Gsα activity in easily accessible cells. This form of PHP is associated with heterozygous inactivating mutations in Gsα-coding exons of GNAS, an imprinted gene locus on chromosome 20q13.3. Patients with PHP-Ib typically have isolated parathyroid hormone resistance, lack AHO features and demonstrate normal erythrocyte Gsα activity. Instead of coding Gsα mutations, patients with PHP-Ib display imprinting defects of GNAS, caused, at least in some cases, by genetic mutations within or nearby this gene.Patients Two unrelated PHP families, each of which includes at least one patient with a Gsα coding mutation and another with GNAS loss of imprinting, are reported here.Results One of the patients with GNAS imprinting defects has paternal uniparental isodisomy of chromosome 20q, explaining the observed imprinting abnormalities. The identified Gsα coding mutations include a tetranucleotide deletion in exon 7, which is frequently found in PHP-Ia, and a novel single nucleotide change at the acceptor splice junction of intron 11.Conclusions These molecular data reveal an interesting mixture, in the same family, of both genetic and epigenetic mutations of the same gene.