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An Pediatr (Barc) ; 74(2): 116-21, 2011 Feb.
Article in Spanish | MEDLINE | ID: mdl-21169072

ABSTRACT

Pseudohypoparathyroidism (PHP) is a heterogeneous group of endocrine diseases characterised by hypocalcaemia, hyperphosphataemia and resistance to PTH. There are different forms of PHP. PHP-Ia is the most frequent form and shows multi-hormonal resistance, GNAS (Gs(α)) mutations and signs of Albright́s hereditary osteodystrophy (AHO). PseudoPHP (PPHP) have isolated AHO without hormonal resistance and it is also caused by GNAS mutations. We present a family that share the same inactivating GNAS mutation (Asn264LysfsX35); the mother being affected with PPHP and the two daughters with PHP-Ia. We discuss the different clinical phenotypes and the dominant mode of inheritance with genetic imprinting where the phenotype of the offspring depends on the sex of the parent affected.


Subject(s)
GTP-Binding Protein alpha Subunits, Gs/genetics , Mutation , Pseudohypoparathyroidism/genetics , Adult , Chromogranins , Female , Humans , Infant, Newborn
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