La parálisis periódica hipocalemia es un trastorno autosómico dominante neuromuscular, que forma parte de un conjunto de enfermedades agrupadas conocidas como canalopatías. Estas diversas patologías se caracterizan por presentar mutaciones en los genes ubicados en los canales iónicos de sodio y calcio dependientes del voltaje, los cuales generan una inexitabilidad de la membrana muscular. Presentan diversas manifestaciones clínicas como episodios de parálisis y debilidad muscular de los cuatro miembros que puede durar horas, no obstante, suelen afectar principalmente a nivel de los miembros inferiores, relacionados con niveles bajos de potasio en sangre. Se describen dos genes causantes de las alteraciones en el voltaje denominados CACNA1S,...
Congenital muscular dystrophy (CMD) composes a group of disorders characterized by hypotonia and mus...
In humans, skeletal muscle channelopathies are genetic disease with very low incidence. Regarding th...
Developmental hip dysplasia is the most common orthopedic disorder in newborns; refers to a wide spe...
La parálisis periódica hipocalemia es un trastorno autosómico dominante neuromuscular, que forma par...
The hipopotasemic tiroxic periodic paralysis is an entity of low frequency, with incidence of 2 % in...
The opsoclonus-myoclonus syndrome is a rare medical condition associated with an autounmmune etiolog...
Duchene muscular Dystrophy is a genetic disease linked to X chromosome, mainly caused by deletions o...
Guyon`s canal in the wrist is a highly complex anatomical area, its limits are formed by various str...
De Morsier syndrome dysplasia septo-optic (DSO), was described by De Morsier in 1956, who recognized...
Multiple sclerosis is the most prevalent, chronic, inflammatory and neurodegenerative disease of the...
Guillain-Barre Syndrome (GBS) is one of the most frequent peripheral neuropathies in the world, whic...
Vitiligo is an autoimmune acquired hypomelanosis, which has an important genetic component and ...
Periodic paralysis is a rare disease, characterized by transient weakness associated with abnormal l...
The PTEN gene, better known as PTEN tyrosine phosphatase, is a tumor suppressor gene on chromosome 1...
Congenital myopathies are a heterogeneous group of muscle diseases of genetic origin, which present ...
Congenital muscular dystrophy (CMD) composes a group of disorders characterized by hypotonia and mus...
In humans, skeletal muscle channelopathies are genetic disease with very low incidence. Regarding th...
Developmental hip dysplasia is the most common orthopedic disorder in newborns; refers to a wide spe...
La parálisis periódica hipocalemia es un trastorno autosómico dominante neuromuscular, que forma par...
The hipopotasemic tiroxic periodic paralysis is an entity of low frequency, with incidence of 2 % in...
The opsoclonus-myoclonus syndrome is a rare medical condition associated with an autounmmune etiolog...
Duchene muscular Dystrophy is a genetic disease linked to X chromosome, mainly caused by deletions o...
Guyon`s canal in the wrist is a highly complex anatomical area, its limits are formed by various str...
De Morsier syndrome dysplasia septo-optic (DSO), was described by De Morsier in 1956, who recognized...
Multiple sclerosis is the most prevalent, chronic, inflammatory and neurodegenerative disease of the...
Guillain-Barre Syndrome (GBS) is one of the most frequent peripheral neuropathies in the world, whic...
Vitiligo is an autoimmune acquired hypomelanosis, which has an important genetic component and ...
Periodic paralysis is a rare disease, characterized by transient weakness associated with abnormal l...
The PTEN gene, better known as PTEN tyrosine phosphatase, is a tumor suppressor gene on chromosome 1...
Congenital myopathies are a heterogeneous group of muscle diseases of genetic origin, which present ...
Congenital muscular dystrophy (CMD) composes a group of disorders characterized by hypotonia and mus...
In humans, skeletal muscle channelopathies are genetic disease with very low incidence. Regarding th...
Developmental hip dysplasia is the most common orthopedic disorder in newborns; refers to a wide spe...