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An Pediatr (Barc) ; 74(2): 116-21, 2011 Feb.
Artigo em Espanhol | MEDLINE | ID: mdl-21169072

RESUMO

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.


Assuntos
Subunidades alfa Gs de Proteínas de Ligação ao GTP/genética , Mutação , Pseudo-Hipoparatireoidismo/genética , Adulto , Cromograninas , Feminino , Humanos , Recém-Nascido
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