Cerebellar ataxia-hypogonadism syndrome

Cerebellar ataxia-hypogonadism syndrome is a very rare autosomal recessive neurodegenerative disorder characterized by the combination of progressive cerebellar ataxia with onset from early childhood to the fourth decade, and hypogonadotropic hypogonadism (delayed puberty and lack of secondary sex characteristics). Cerebellar ataxia-hypogonadism syndrome belongs to a clinical continuum of neurodegenerative disorders along with clinically overlapping disorders such as ataxia-hypogonadism-choroidal dystrophy syndrome.

Also known as: Gordon-Holmes syndrome, luteinizing hormone-releasing hormone deficiency with ataxia, GDHS, Gordon Holmes syndrome, LHRH deficiency and ataxia, cerebellar ataxia - hypogonadism, cerebellar ataxia and hypogonadotropic hypogonadism, luteinizing hormone releasing hormone, deficiency of with ataxia

0 clinical trials for this condition and its sub-types, 0 tagged with Cerebellar ataxia-hypogonadism syndrome itself.