SciELO - Scientific Electronic Library Online

 
vol.20 issue4The effect of the aqueous extract of "Mashua" Tropaeolum Tuberosum on sperm quality and its implication in preimplantation embryonic development. Pre-Clinical testThe use of chest computed tomography scan in the context of the Sars-Cov-2 pandemic author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

  • Have no cited articlesCited by SciELO

Related links

  • Have no similar articlesSimilars in SciELO

Share


Revista de la Facultad de Medicina Humana

Print version ISSN 1814-5469On-line version ISSN 2308-0531

Abstract

CASTRO-MUJICA, María del Carmen  and  ABARCA-BARRIGA, Hugo. Genetic bases of pulmonary arterial hypertension. Rev. Fac. Med. Hum. [online]. 2020, vol.20, n.4, pp.670-681. ISSN 1814-5469.  http://dx.doi.org/10.25176/rfmh.v20i4.2946.

Pulmonary arterial hypertension (PAH) is a heterogeneous disease where genes play an extremely important role. Hereditary PAH (hAPH) is defined as a genetic condition with an autosomal dominant inheritance pattern, incomplete penetrance, variable expressiveness, presenting an anticipatory phenomenon and grouping cases of familial PAH defined by the presence of two or more members of the family with PAH with or without identified germline variant and idiopathic PAH cases corresponding to isolated cases in the family with an identified germline variant. To establish the diagnosis of hAPH, it is necessary to confirm the diagnosis in at least two relatives (fHAP) or to identify the germline variant in an isolated case in the family (HAPi).

Keywords : Pulmonary hypertension; Genetic counseling (Source: MeSH NLM)..

        · abstract in Spanish     · text in English | Spanish     · English ( pdf ) | Spanish ( pdf )