120 top medical experts on Cerebellar Ataxia and Hypogonadotropic Hypogonadism across 11 countries and 1 U.S. states, including 6 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Cerebellar Ataxia and Hypogonadotropic Hypogonadism: 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 (see this term).
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Gordon Holmes Syndrome,  LHRH Deficiency and Ataxia,  with Ataxia Deficiency of Luteinizing Hormone-Releasing Hormone


  

        

                    


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