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Rev. obstet. ginecol. Venezuela ; 75(4): 280-283, dic. 2015.
Article in Spanish | LILACS | ID: lil-783110

ABSTRACT

Presentamos el caso de una paciente de 35 años de edad, VII gestas, VI molas I aborto, portadora de la mutación en la proteína NLRP7, evaluada en el servicio de patología del primer trimestre del embarazo de la Maternidad “Concepción Palacios” entre los años 1998- 2010. Ambos padres tenían cariotipos normales y se detectó un antecedente familiar de embarazo molar. Este caso forma parte de un raro subconjunto de molas cuyo origen es biparental, generalmente recurrente y a menudo familiar y se asocia a imposibilidad de obtener un embarazo exitoso.


We report the case of a 35 years old patient, with 7 pregnancies, 6 molas, 1 abortion, carrier of a mutation in the protein NLRP7, evaluated in the pathology service of the Maternidad “Concepcion Palacios” between 1998-2010. Both parents had normal karyotypes and a family history of molar pregnancy was detected. This case is part of a rare subset of molas with biparental origin, usually recurrent and often family and associated with failure to obtain a successful pregnancy.


Subject(s)
Humans , Male , Female , Pregnancy , Pregnancy Complications , Hydatidiform Mole , Incidence , Gestational Trophoblastic Disease , Hyperplasia , Risk Factors , Genes
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