Cerebellar ataxia and hypogonadotropic hypogonadism
Other Names: Cerebellar ataxia - hypogonadism; Luteinizing hormone-releasing hormone deficiency with ataxia; Luteinizing hormone releasing hormone, deficiency of with ataxia; LHRH deficiency and ataxia; Gordon-Holmes syndrome; 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 .
NIH genetic and rare disease info[edit source]
Cerebellar ataxia and hypogonadotropic hypogonadism is a rare disease.
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